Canonical Allele Identifier: CA1685226431
Gene: PMS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5986901T= , CM000669.2:g.5986901T= GRCh38
NC_000007.13:g.6026532T= , CM000669.1:g.6026532T= GRCh37
NC_000007.12:g.5993058T= NCBI36
NG_008466.1:g.27206A= , LRG_161:g.27206A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000699814.2:c.*1260A= ENSP00000514615.2:n.*1260A=
ENST00000699840.2:c.1861A= ENSP00000514638.2:p.Met621=
ENST00000699930.2:c.1756A= ENSP00000514695.2:p.Met586=
ENST00000406569.8:c.1678+186A= ENSP00000514464.1:n.1678+186A=
ENST00000644110.2:c.*1458A= ENSP00000496392.2:n.*1458A=
ENST00000699752.1:c.1708A= ENSP00000514561.1:p.Met570=
ENST00000699753.1:c.*1285A= ENSP00000514562.1:n.*1285A=
ENST00000699754.1:c.1666A= ENSP00000514563.1:p.Met556=
ENST00000699755.1:c.*1263A= ENSP00000514564.1:n.*1263A=
ENST00000699756.1:c.*1451A= ENSP00000514565.1:n.*1451A=
ENST00000699757.1:c.*1121A= ENSP00000514566.1:n.*1121A=
ENST00000699758.1:c.*1121A= ENSP00000514567.1:n.*1121A=
ENST00000699759.1:n.2718A=
ENST00000699760.1:c.1546A= ENSP00000514568.1:p.Met516=
ENST00000699761.1:c.1459A= ENSP00000514569.1:p.Met487=
ENST00000699762.1:c.1291A= ENSP00000514570.1:p.Met431=
ENST00000699763.1:c.*954A= ENSP00000514571.1:n.*954A=
ENST00000699764.1:c.*182A= ENSP00000514572.1:n.*182A=
ENST00000699765.1:c.*960A= ENSP00000514573.1:n.*960A=
ENST00000699766.1:c.1864A= ENSP00000514574.1:p.Met622=
ENST00000699767.1:c.1864A= ENSP00000514575.1:p.Met622=
ENST00000699768.1:c.1864A= ENSP00000514576.1:p.Met622=
ENST00000699811.1:c.1459A= ENSP00000514614.1:p.Met487=
ENST00000699813.1:n.1977A=
ENST00000699814.1:c.1487A=
ENST00000699815.1:c.*1395A= ENSP00000514616.1:n.*1395A=
ENST00000699816.1:c.*754A= ENSP00000514617.1:n.*754A=
ENST00000699817.1:c.*1458A= ENSP00000514618.1:n.*1458A=
ENST00000699818.1:c.1459A= ENSP00000514619.1:p.Met487=
ENST00000699819.1:c.*1021A= ENSP00000514620.1:n.*1021A=
ENST00000699820.1:c.1144+2899A= ENSP00000514621.1:n.1144+2899A=
ENST00000699821.1:c.1459A= ENSP00000514622.1:p.Met487=
ENST00000699822.1:c.*1316A= ENSP00000514623.1:n.*1316A=
ENST00000699823.1:c.1459A= ENSP00000514624.1:p.Met487=
ENST00000699824.1:c.*1367A= ENSP00000514625.1:n.*1367A=
ENST00000699825.1:c.1303A= ENSP00000514626.1:p.Met435=
ENST00000699826.1:c.*1263A= ENSP00000514627.1:n.*1263A=
ENST00000699827.1:c.1696A= ENSP00000514628.1:p.Met566=
ENST00000699828.1:c.*954A= ENSP00000514629.1:n.*954A=
ENST00000699833.1:n.3636A=
ENST00000699837.1:c.1459A= ENSP00000514635.1:p.Met487=
ENST00000699838.1:c.*1764A= ENSP00000514636.1:n.*1764A=
ENST00000699839.1:c.2050A= ENSP00000514637.1:p.Met684=
ENST00000699916.1:c.*1121A= ENSP00000514684.1:n.*1121A=
ENST00000699917.1:c.*1313A= ENSP00000514685.1:n.*1313A=
ENST00000699918.1:c.*1365A= ENSP00000514686.1:n.*1365A=
ENST00000699919.1:c.*1451A= ENSP00000514687.1:n.*1451A=
ENST00000699920.1:c.*1500A= ENSP00000514688.1:n.*1500A=
ENST00000699928.1:c.989-3910A= ENSP00000514693.1:n.989-3910A=
ENST00000699951.1:c.*960A= ENSP00000514706.1:n.*960A=
ENST00000699952.1:c.803+10425A= ENSP00000514707.1:n.803+10425A=
ENST00000265849.12:c.1864A= MANE Select ENSP00000265849.7:p.Met622=
ENST00000642292.1:c.1459A= ENSP00000495524.1:p.Met487=
ENST00000642456.1:c.1459A= ENSP00000493814.1:p.Met487=
ENST00000643595.1:c.*1263A= ENSP00000494497.1:n.*1263A=
ENST00000644110.1:c.1546A= ENSP00000496392.1:p.Met516=
ENST00000265849.11:c.1864A= ENSP00000265849.7:p.Met622=
ENST00000382321.5:c.804-3910A= ENSP00000371758.4:n.804-3910A=
ENST00000406569.7:n.1678+186A=
ENST00000441476.6:c.1546A= ENSP00000392843.2:p.Met516=
ENST00000469652.1:n.63-3996A=
NM_000535.5:c.1864A= , LRG_161t1:c.1864A= NP_000526.1:p.Met622=
NR_003085.2:n.1946A=
XM_006715742.2:c.1858A= XP_006715805.1:p.Met620=
XM_006715744.2:c.931A= XP_006715807.1:p.Met311=
XM_011515427.1:c.1909A= XP_011513729.1:p.Met637=
XM_011515428.1:c.1753A= XP_011513730.1:p.Met585=
XM_011515429.1:c.1546A= XP_011513731.1:p.Met516=
XM_011515430.1:c.1546A= XP_011513732.1:p.Met516=
NM_000535.6:c.1864A= NP_000526.2:p.Met622=
NM_001322003.1:c.1459A= NP_001308932.1:p.Met487=
NM_001322004.1:c.1459A= NP_001308933.1:p.Met487=
NM_001322005.1:c.1459A= NP_001308934.1:p.Met487=
NM_001322006.1:c.1708A= NP_001308935.1:p.Met570=
NM_001322007.1:c.1546A= NP_001308936.1:p.Met516=
NM_001322008.1:c.1546A= NP_001308937.1:p.Met516=
NM_001322009.1:c.1459A= NP_001308938.1:p.Met487=
NM_001322010.1:c.1303A= NP_001308939.1:p.Met435=
NM_001322011.1:c.931A= NP_001308940.1:p.Met311=
NM_001322012.1:c.931A= NP_001308941.1:p.Met311=
NM_001322013.1:c.1291A= NP_001308942.1:p.Met431=
NM_001322014.1:c.1864A= NP_001308943.1:p.Met622=
NM_001322015.1:c.1555A= NP_001308944.1:p.Met519=
NR_136154.1:n.1951A=
XM_006715744.4:c.931A= XP_006715807.1:p.Met311=
XM_017012342.2:c.931A= XP_016867831.1:p.Met311=
XM_024446800.1:c.1303A= XP_024302568.1:p.Met435=
NM_000535.7:c.1864A= MANE Select NP_000526.2:p.Met622=
NM_001322003.2:c.1459A= NP_001308932.1:p.Met487=
NM_001322004.2:c.1459A= NP_001308933.1:p.Met487=
NM_001322005.2:c.1459A= NP_001308934.1:p.Met487=
NM_001322006.2:c.1708A= NP_001308935.1:p.Met570=
NM_001322008.2:c.1546A= NP_001308937.1:p.Met516=
NM_001322009.2:c.1459A= NP_001308938.1:p.Met487=
NM_001322010.2:c.1303A= NP_001308939.1:p.Met435=
NM_001322011.2:c.931A= NP_001308940.1:p.Met311=
NM_001322012.2:c.931A= NP_001308941.1:p.Met311=
NM_001322013.2:c.1291A= NP_001308942.1:p.Met431=
NM_001322014.2:c.1864A= NP_001308943.1:p.Met622=
NM_001322015.2:c.1555A= NP_001308944.1:p.Met519=
NM_001322007.2:c.1546A= NP_001308936.1:p.Met516=