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. 2021 Sep 16;413(29):7241–7249. doi: 10.1007/s00216-021-03649-1

Table 2.

Major coronavirus variants of concern, mutation sites in surface spike protein and unique peptide masses that distinguish such strains

Lineage Origin Mutations Tryptic + GluC segmenta Sequence (mutations shown underlined, except deletions)b Mass [M + H]+ mono. Strain distinguishing peptide massesc
B.1.17 (Alpha) UK HV69–70 del. 54–77 minus 69–70 LFLPFFSNVTWFHAISGTNGTK 2484.2711 2484.2711
Y144 del. 139–147 minus 144 PFLGVYHK 960.5302 960.5302
N501Y 499–504 STYLVK 710.4084
A570D 569–570 ID 247.1289 (247.1289)
D614G 587–619 ITPCSFGGVSVITPGTNTSNQVAVLYQGVNCTE 3356.6138
P681H 664–682 IPIGAGICASYQTQTNSHR 2016.9920 2016.9920
T716I 703–725 NSVAYSNNSIAIPINFTISVTTE 2455.2352 2455.2352
S982A 979–982 ILAR 472.3242 (472.3242)
D1118H 1112–1127 PQIITTHNTFVSGNCD 1746.8116 1746.8116
B.1.351 (Beta) South Africa L18F 1–21 MFVFLVLLPLVSSQCVNFTTR 2414.2975
D80A 79–88 FANPVLPFND 1133.5626 1133.5626
D215G 215–224 GLPQGFSALE 1018.5204 1018.5204
LAL 242–244 del. 238–246 minus 242–244 FQTLHR 801.4366 801.4366
R246I 238–253 FQTLLALHISYLTPGD 1788.9531 1788.9531
K417N 409–419 QIAPGQTGNIAD 1184.5906 1184.5906
E484K 472–484 IYQAGSTPCNGVK 1337.6519 1337.6519
N501Y 499–504 STYLVK 710.4084
D614G 587–619 ITPCSFGGVSVITPGTNTSNQVAVLYQGVNCTE 3356.6138
A701V 686–702 SVASQSIIAYTMSLGVE 1755.8834 1755.8834
B.1.617 (Delta) India T95I 89–96 GVYFASIE 885.4353 885.4353
G142D 139–142 PFLD 491.2501
E154K 151–154 SWMK 551.2647 551.2647
L452R 429–452 FTGCVIAWNSNNR 1481.6955
E484Q 472–509 IYQAGSTPCNGVQGFNCYFPLQSYGFQPTNGVGYQPYR 4221.9222 4221.9222
D614G 587–619 ITPCSFGGVSVITPGTNTSNQVAVLYQGVNCTE 3356.6138
P681R 664–681 IPIGAGICASYQTQTNSR 1879.9331
B.1.617.2 (Delta plus) India T19R 1–19 MFVFLVLLPLVSSQCVNLR 2178.2178 2178.2178
G142D 139–142 PFLD 491.2501
EF156–157 del. 155–158 minus 156–157 SR 262.1510 (262.1510)
R158G 154–169 SEFGVYSSANNCTFE 1654.6690 1654.6690
L452R 429–452 FTGCVIAWNSNNR 1481.6955
T478K 472–478 IYQAGSK 766.4094 766.4094
D614G 587–619 ITPCSFGGVSVITPGTNTSNQVAVLYQGVNCTE 3356.6138
P681R 664–681 IPIGAGICASYQTQTNSR 1879.9331
D950N 948–964 LQNVVNQNAQALNTLVK 1867.0396 1867.0396
P.1 (Gamma) Brazil L18F 1–21 MFVFLVLLPLVSSQCVNFTTR 2414.2975
T20N 1–21 MFVFLVLLPLVSSQCVNLTNR 2393.3084 2393.3084
P26S 22–34 TQLPSAYTNSFTR 1485.7333 1485.7333
D138Y 133–147 FQFCNYPFLGVYYHK 1925.9043 1925.9043
R190S 188–191 NLSE 462.2195 (462.2195)
K417T 409–420 QIAPGQTGTIAD 1171.5954 1171.5954
E484K 472–484 IYQAGSTPCNGVK 1337.6519 1337.6519
N501Y 499–504 STYLVK 710.4084 710.4084
D614G 587–619 ITPCSFGGVSVITPGTNTSNQVAVLYQGVNCTE 3356.6138
H655Y 655–661 YVNNSYE 888.3734 888.3734
T1027I 1019–1028 ASANLAAIK 858.5044 858.5044
V1176F 1169–1181 ISGINASFVNIQK 1390.7689 1390.7689

aResidue numbering is based on the originating strain and may differ in some variants due to the presence of deletion sites

bAll strain distinguishing peptides do not contain proline (F817P, A892P, A899P, A942P, K986P, V987P) or alanine substitutions (R683A and R685A) added to the recombinant forms for the variants introduced to stabilize the S-protein trimer

cThose with masses lower than 500 are bracketed since they typically appear among matrix background ions in MALDI mass spectra. All other peptides differ in mass by at least 83 ppm, as is the case for mass 1133.5626 and that of 1133.6565 for missed cleaved peptide 821–830 (of sequence LLFNKVTLAD) for the spike protein of the original reference strain