Canonical Allele Identifier: CA366741757
Gene: PMS2 HGNC NCBI

Linked Data

dbSNP Id: rs2128729230

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5987263A>G , CM000669.2:g.5987263A>G GRCh38
NC_000007.13:g.6026894A>G , CM000669.1:g.6026894A>G GRCh37
NC_000007.12:g.5993420A>G NCBI36
NG_008466.1:g.26844T>C , LRG_161:g.26844T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000699814.2:c.*898T>C ENSP00000514615.2:n.*898T>C
ENST00000699840.2:c.1499T>C ENSP00000514638.2:p.Val500Ala
ENST00000699930.2:c.1394T>C ENSP00000514695.2:p.Val465Ala
ENST00000406569.8:c.1502T>C ENSP00000514464.1:p.Val501Ala
ENST00000644110.2:c.*1096T>C ENSP00000496392.2:n.*1096T>C
ENST00000699752.1:c.1346T>C ENSP00000514561.1:p.Val449Ala
ENST00000699753.1:c.*923T>C ENSP00000514562.1:n.*923T>C
ENST00000699754.1:c.1304T>C ENSP00000514563.1:p.Val435Ala
ENST00000699755.1:c.*901T>C ENSP00000514564.1:n.*901T>C
ENST00000699756.1:c.*1089T>C ENSP00000514565.1:n.*1089T>C
ENST00000699757.1:c.*759T>C ENSP00000514566.1:n.*759T>C
ENST00000699758.1:c.*759T>C ENSP00000514567.1:n.*759T>C
ENST00000699759.1:n.2356T>C
ENST00000699760.1:c.1184T>C ENSP00000514568.1:p.Val395Ala
ENST00000699761.1:c.1097T>C ENSP00000514569.1:p.Val366Ala
ENST00000699762.1:c.929T>C ENSP00000514570.1:p.Val310Ala
ENST00000699763.1:c.*592T>C ENSP00000514571.1:n.*592T>C
ENST00000699764.1:c.1502T>C ENSP00000514572.1:p.Val501Ala
ENST00000699765.1:c.*598T>C ENSP00000514573.1:n.*598T>C
ENST00000699766.1:c.1502T>C ENSP00000514574.1:p.Val501Ala
ENST00000699767.1:c.1502T>C ENSP00000514575.1:p.Val501Ala
ENST00000699768.1:c.1502T>C ENSP00000514576.1:p.Val501Ala
ENST00000699811.1:c.1097T>C ENSP00000514614.1:p.Val366Ala
ENST00000699813.1:n.1615T>C
ENST00000699814.1:c.1125T>C
ENST00000699815.1:c.*1033T>C ENSP00000514616.1:n.*1033T>C
ENST00000699816.1:c.*392T>C ENSP00000514617.1:n.*392T>C
ENST00000699817.1:c.*1096T>C ENSP00000514618.1:n.*1096T>C
ENST00000699818.1:c.1097T>C ENSP00000514619.1:p.Val366Ala
ENST00000699819.1:c.*659T>C ENSP00000514620.1:n.*659T>C
ENST00000699820.1:c.1144+2537T>C ENSP00000514621.1:n.1144+2537T>C
ENST00000699821.1:c.1097T>C ENSP00000514622.1:p.Val366Ala
ENST00000699822.1:c.*954T>C ENSP00000514623.1:n.*954T>C
ENST00000699823.1:c.1097T>C ENSP00000514624.1:p.Val366Ala
ENST00000699824.1:c.*1005T>C ENSP00000514625.1:n.*1005T>C
ENST00000699825.1:c.941T>C ENSP00000514626.1:p.Val314Ala
ENST00000699826.1:c.*901T>C ENSP00000514627.1:n.*901T>C
ENST00000699827.1:c.1334T>C ENSP00000514628.1:p.Val445Ala
ENST00000699828.1:c.*592T>C ENSP00000514629.1:n.*592T>C
ENST00000699833.1:n.3274T>C
ENST00000699837.1:c.1097T>C ENSP00000514635.1:p.Val366Ala
ENST00000699838.1:c.*1402T>C ENSP00000514636.1:n.*1402T>C
ENST00000699839.1:c.1688T>C ENSP00000514637.1:p.Val563Ala
ENST00000699916.1:c.*759T>C ENSP00000514684.1:n.*759T>C
ENST00000699917.1:c.*951T>C ENSP00000514685.1:n.*951T>C
ENST00000699918.1:c.*1003T>C ENSP00000514686.1:n.*1003T>C
ENST00000699919.1:c.*1089T>C ENSP00000514687.1:n.*1089T>C
ENST00000699920.1:c.*1138T>C ENSP00000514688.1:n.*1138T>C
ENST00000699928.1:c.989-4272T>C ENSP00000514693.1:n.989-4272T>C
ENST00000699929.1:c.*803T>C ENSP00000514694.1:n.*803T>C
ENST00000699930.1:c.1394T>C ENSP00000514695.1:p.Val465Ala
ENST00000699931.1:n.2930T>C
ENST00000699951.1:c.*598T>C ENSP00000514706.1:n.*598T>C
ENST00000699952.1:c.803+10063T>C ENSP00000514707.1:n.803+10063T>C
ENST00000699953.1:c.*609T>C ENSP00000514708.1:n.*609T>C
ENST00000699954.1:c.*803T>C ENSP00000514709.1:n.*803T>C
ENST00000265849.12:c.1502T>C MANE Select ENSP00000265849.7:p.Val501Ala
ENST00000642292.1:c.1097T>C ENSP00000495524.1:p.Val366Ala
ENST00000642456.1:c.1097T>C ENSP00000493814.1:p.Val366Ala
ENST00000643595.1:c.*901T>C ENSP00000494497.1:n.*901T>C
ENST00000644110.1:c.1184T>C ENSP00000496392.1:p.Val395Ala
ENST00000265849.11:c.1502T>C ENSP00000265849.7:p.Val501Ala
ENST00000382321.5:c.804-4272T>C ENSP00000371758.4:n.804-4272T>C
ENST00000406569.7:n.1502T>C
ENST00000441476.6:c.1184T>C ENSP00000392843.2:p.Val395Ala
ENST00000469652.1:n.63-4358T>C
NM_000535.5:c.1502T>C , LRG_161t1:c.1502T>C NP_000526.1:p.Val501Ala
NR_003085.2:n.1584T>C
XM_006715742.2:c.1496T>C XP_006715805.1:p.Val499Ala
XM_006715744.2:c.569T>C XP_006715807.1:p.Val190Ala
XM_011515427.1:c.1547T>C XP_011513729.1:p.Val516Ala
XM_011515428.1:c.1391T>C XP_011513730.1:p.Val464Ala
XM_011515429.1:c.1184T>C XP_011513731.1:p.Val395Ala
XM_011515430.1:c.1184T>C XP_011513732.1:p.Val395Ala
NM_000535.6:c.1502T>C NP_000526.2:p.Val501Ala
NM_001322003.1:c.1097T>C NP_001308932.1:p.Val366Ala
NM_001322004.1:c.1097T>C NP_001308933.1:p.Val366Ala
NM_001322005.1:c.1097T>C NP_001308934.1:p.Val366Ala
NM_001322006.1:c.1346T>C NP_001308935.1:p.Val449Ala
NM_001322007.1:c.1184T>C NP_001308936.1:p.Val395Ala
NM_001322008.1:c.1184T>C NP_001308937.1:p.Val395Ala
NM_001322009.1:c.1097T>C NP_001308938.1:p.Val366Ala
NM_001322010.1:c.941T>C NP_001308939.1:p.Val314Ala
NM_001322011.1:c.569T>C NP_001308940.1:p.Val190Ala
NM_001322012.1:c.569T>C NP_001308941.1:p.Val190Ala
NM_001322013.1:c.929T>C NP_001308942.1:p.Val310Ala
NM_001322014.1:c.1502T>C NP_001308943.1:p.Val501Ala
NM_001322015.1:c.1193T>C NP_001308944.1:p.Val398Ala
NR_136154.1:n.1589T>C
XM_006715744.4:c.569T>C XP_006715807.1:p.Val190Ala
XM_017012342.2:c.569T>C XP_016867831.1:p.Val190Ala
XM_024446800.1:c.941T>C XP_024302568.1:p.Val314Ala
NM_000535.7:c.1502T>C MANE Select NP_000526.2:p.Val501Ala
NM_001322003.2:c.1097T>C NP_001308932.1:p.Val366Ala
NM_001322004.2:c.1097T>C NP_001308933.1:p.Val366Ala
NM_001322005.2:c.1097T>C NP_001308934.1:p.Val366Ala
NM_001322006.2:c.1346T>C NP_001308935.1:p.Val449Ala
NM_001322008.2:c.1184T>C NP_001308937.1:p.Val395Ala
NM_001322009.2:c.1097T>C NP_001308938.1:p.Val366Ala
NM_001322010.2:c.941T>C NP_001308939.1:p.Val314Ala
NM_001322011.2:c.569T>C NP_001308940.1:p.Val190Ala
NM_001322012.2:c.569T>C NP_001308941.1:p.Val190Ala
NM_001322013.2:c.929T>C NP_001308942.1:p.Val310Ala
NM_001322014.2:c.1502T>C NP_001308943.1:p.Val501Ala
NM_001322015.2:c.1193T>C NP_001308944.1:p.Val398Ala
NM_001322007.2:c.1184T>C NP_001308936.1:p.Val395Ala