Canonical Allele Identifier: CA366739523
Gene: PMS2 HGNC NCBI

Linked Data

dbSNP Id: rs1218276502

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5986900A>T , CM000669.2:g.5986900A>T GRCh38
NC_000007.13:g.6026531A>T , CM000669.1:g.6026531A>T GRCh37
NC_000007.12:g.5993057A>T NCBI36
NG_008466.1:g.27207T>A , LRG_161:g.27207T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000699814.2:c.*1261T>A ENSP00000514615.2:n.*1261T>A
ENST00000699840.2:c.1862T>A ENSP00000514638.2:p.Met621Lys
ENST00000699930.2:c.1757T>A ENSP00000514695.2:p.Met586Lys
ENST00000406569.8:c.1678+187T>A ENSP00000514464.1:n.1678+187T>A
ENST00000644110.2:c.*1459T>A ENSP00000496392.2:n.*1459T>A
ENST00000699752.1:c.1709T>A ENSP00000514561.1:p.Met570Lys
ENST00000699753.1:c.*1286T>A ENSP00000514562.1:n.*1286T>A
ENST00000699754.1:c.1667T>A ENSP00000514563.1:p.Met556Lys
ENST00000699755.1:c.*1264T>A ENSP00000514564.1:n.*1264T>A
ENST00000699756.1:c.*1452T>A ENSP00000514565.1:n.*1452T>A
ENST00000699757.1:c.*1122T>A ENSP00000514566.1:n.*1122T>A
ENST00000699758.1:c.*1122T>A ENSP00000514567.1:n.*1122T>A
ENST00000699759.1:n.2719T>A
ENST00000699760.1:c.1547T>A ENSP00000514568.1:p.Met516Lys
ENST00000699761.1:c.1460T>A ENSP00000514569.1:p.Met487Lys
ENST00000699762.1:c.1292T>A ENSP00000514570.1:p.Met431Lys
ENST00000699763.1:c.*955T>A ENSP00000514571.1:n.*955T>A
ENST00000699764.1:c.*183T>A ENSP00000514572.1:n.*183T>A
ENST00000699765.1:c.*961T>A ENSP00000514573.1:n.*961T>A
ENST00000699766.1:c.1865T>A ENSP00000514574.1:p.Met622Lys
ENST00000699767.1:c.1865T>A ENSP00000514575.1:p.Met622Lys
ENST00000699768.1:c.1865T>A ENSP00000514576.1:p.Met622Lys
ENST00000699811.1:c.1460T>A ENSP00000514614.1:p.Met487Lys
ENST00000699813.1:n.1978T>A
ENST00000699814.1:c.1488T>A
ENST00000699815.1:c.*1396T>A ENSP00000514616.1:n.*1396T>A
ENST00000699816.1:c.*755T>A ENSP00000514617.1:n.*755T>A
ENST00000699817.1:c.*1459T>A ENSP00000514618.1:n.*1459T>A
ENST00000699818.1:c.1460T>A ENSP00000514619.1:p.Met487Lys
ENST00000699819.1:c.*1022T>A ENSP00000514620.1:n.*1022T>A
ENST00000699820.1:c.1144+2900T>A ENSP00000514621.1:n.1144+2900T>A
ENST00000699821.1:c.1460T>A ENSP00000514622.1:p.Met487Lys
ENST00000699822.1:c.*1317T>A ENSP00000514623.1:n.*1317T>A
ENST00000699823.1:c.1460T>A ENSP00000514624.1:p.Met487Lys
ENST00000699824.1:c.*1368T>A ENSP00000514625.1:n.*1368T>A
ENST00000699825.1:c.1304T>A ENSP00000514626.1:p.Met435Lys
ENST00000699826.1:c.*1264T>A ENSP00000514627.1:n.*1264T>A
ENST00000699827.1:c.1697T>A ENSP00000514628.1:p.Met566Lys
ENST00000699828.1:c.*955T>A ENSP00000514629.1:n.*955T>A
ENST00000699833.1:n.3637T>A
ENST00000699837.1:c.1460T>A ENSP00000514635.1:p.Met487Lys
ENST00000699838.1:c.*1765T>A ENSP00000514636.1:n.*1765T>A
ENST00000699839.1:c.2051T>A ENSP00000514637.1:p.Met684Lys
ENST00000699916.1:c.*1122T>A ENSP00000514684.1:n.*1122T>A
ENST00000699917.1:c.*1314T>A ENSP00000514685.1:n.*1314T>A
ENST00000699918.1:c.*1366T>A ENSP00000514686.1:n.*1366T>A
ENST00000699919.1:c.*1452T>A ENSP00000514687.1:n.*1452T>A
ENST00000699920.1:c.*1501T>A ENSP00000514688.1:n.*1501T>A
ENST00000699928.1:c.989-3909T>A ENSP00000514693.1:n.989-3909T>A
ENST00000699951.1:c.*961T>A ENSP00000514706.1:n.*961T>A
ENST00000699952.1:c.803+10426T>A ENSP00000514707.1:n.803+10426T>A
ENST00000265849.12:c.1865T>A MANE Select ENSP00000265849.7:p.Met622Lys
ENST00000642292.1:c.1460T>A ENSP00000495524.1:p.Met487Lys
ENST00000642456.1:c.1460T>A ENSP00000493814.1:p.Met487Lys
ENST00000643595.1:c.*1264T>A ENSP00000494497.1:n.*1264T>A
ENST00000644110.1:c.1547T>A ENSP00000496392.1:p.Met516Lys
ENST00000265849.11:c.1865T>A ENSP00000265849.7:p.Met622Lys
ENST00000382321.5:c.804-3909T>A ENSP00000371758.4:n.804-3909T>A
ENST00000406569.7:n.1678+187T>A
ENST00000441476.6:c.1547T>A ENSP00000392843.2:p.Met516Lys
ENST00000469652.1:n.63-3995T>A
NM_000535.5:c.1865T>A , LRG_161t1:c.1865T>A NP_000526.1:p.Met622Lys
NR_003085.2:n.1947T>A
XM_006715742.2:c.1859T>A XP_006715805.1:p.Met620Lys
XM_006715744.2:c.932T>A XP_006715807.1:p.Met311Lys
XM_011515427.1:c.1910T>A XP_011513729.1:p.Met637Lys
XM_011515428.1:c.1754T>A XP_011513730.1:p.Met585Lys
XM_011515429.1:c.1547T>A XP_011513731.1:p.Met516Lys
XM_011515430.1:c.1547T>A XP_011513732.1:p.Met516Lys
NM_000535.6:c.1865T>A NP_000526.2:p.Met622Lys
NM_001322003.1:c.1460T>A NP_001308932.1:p.Met487Lys
NM_001322004.1:c.1460T>A NP_001308933.1:p.Met487Lys
NM_001322005.1:c.1460T>A NP_001308934.1:p.Met487Lys
NM_001322006.1:c.1709T>A NP_001308935.1:p.Met570Lys
NM_001322007.1:c.1547T>A NP_001308936.1:p.Met516Lys
NM_001322008.1:c.1547T>A NP_001308937.1:p.Met516Lys
NM_001322009.1:c.1460T>A NP_001308938.1:p.Met487Lys
NM_001322010.1:c.1304T>A NP_001308939.1:p.Met435Lys
NM_001322011.1:c.932T>A NP_001308940.1:p.Met311Lys
NM_001322012.1:c.932T>A NP_001308941.1:p.Met311Lys
NM_001322013.1:c.1292T>A NP_001308942.1:p.Met431Lys
NM_001322014.1:c.1865T>A NP_001308943.1:p.Met622Lys
NM_001322015.1:c.1556T>A NP_001308944.1:p.Met519Lys
NR_136154.1:n.1952T>A
XM_006715744.4:c.932T>A XP_006715807.1:p.Met311Lys
XM_017012342.2:c.932T>A XP_016867831.1:p.Met311Lys
XM_024446800.1:c.1304T>A XP_024302568.1:p.Met435Lys
NM_000535.7:c.1865T>A MANE Select NP_000526.2:p.Met622Lys
NM_001322003.2:c.1460T>A NP_001308932.1:p.Met487Lys
NM_001322004.2:c.1460T>A NP_001308933.1:p.Met487Lys
NM_001322005.2:c.1460T>A NP_001308934.1:p.Met487Lys
NM_001322006.2:c.1709T>A NP_001308935.1:p.Met570Lys
NM_001322008.2:c.1547T>A NP_001308937.1:p.Met516Lys
NM_001322009.2:c.1460T>A NP_001308938.1:p.Met487Lys
NM_001322010.2:c.1304T>A NP_001308939.1:p.Met435Lys
NM_001322011.2:c.932T>A NP_001308940.1:p.Met311Lys
NM_001322012.2:c.932T>A NP_001308941.1:p.Met311Lys
NM_001322013.2:c.1292T>A NP_001308942.1:p.Met431Lys
NM_001322014.2:c.1865T>A NP_001308943.1:p.Met622Lys
NM_001322015.2:c.1556T>A NP_001308944.1:p.Met519Lys
NM_001322007.2:c.1547T>A NP_001308936.1:p.Met516Lys