Canonical Allele Identifier: CA1685217696
Gene: PMS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5982935A= , CM000669.2:g.5982935A= GRCh38
NC_000007.13:g.6022566A= , CM000669.1:g.6022566A= GRCh37
NC_000007.12:g.5989092A= NCBI36
NG_008466.1:g.31172T= , LRG_161:g.31172T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000699814.2:c.*1459T= ENSP00000514615.2:n.*1459T=
ENST00000699840.2:c.2060T= ENSP00000514638.2:p.Ile687=
ENST00000699930.2:c.1955T= ENSP00000514695.2:p.Ile652=
ENST00000406569.8:c.1678+4152T= ENSP00000514464.1:n.1678+4152T=
ENST00000644110.2:c.*1657T= ENSP00000496392.2:n.*1657T=
ENST00000699752.1:c.1907T= ENSP00000514561.1:p.Ile636=
ENST00000699753.1:c.*1484T= ENSP00000514562.1:n.*1484T=
ENST00000699754.1:c.1865T= ENSP00000514563.1:p.Ile622=
ENST00000699755.1:c.*1462T= ENSP00000514564.1:n.*1462T=
ENST00000699756.1:c.*1650T= ENSP00000514565.1:n.*1650T=
ENST00000699757.1:c.*1320T= ENSP00000514566.1:n.*1320T=
ENST00000699758.1:c.*1320T= ENSP00000514567.1:n.*1320T=
ENST00000699759.1:n.2917T=
ENST00000699760.1:c.1745T= ENSP00000514568.1:p.Ile582=
ENST00000699761.1:c.1658T= ENSP00000514569.1:p.Ile553=
ENST00000699762.1:c.1490T= ENSP00000514570.1:p.Ile497=
ENST00000699763.1:c.*1153T= ENSP00000514571.1:n.*1153T=
ENST00000699764.1:c.*381T= ENSP00000514572.1:n.*381T=
ENST00000699765.1:c.*1159T= ENSP00000514573.1:n.*1159T=
ENST00000699766.1:c.2063T= ENSP00000514574.1:p.Ile688=
ENST00000699767.1:c.2063T= ENSP00000514575.1:p.Ile688=
ENST00000699768.1:c.2063T= ENSP00000514576.1:p.Ile688=
ENST00000699811.1:c.1658T= ENSP00000514614.1:p.Ile553=
ENST00000699813.1:n.2176T=
ENST00000699814.1:c.1686T=
ENST00000699815.1:c.*1594T= ENSP00000514616.1:n.*1594T=
ENST00000699816.1:c.*953T= ENSP00000514617.1:n.*953T=
ENST00000699817.1:c.*1657T= ENSP00000514618.1:n.*1657T=
ENST00000699818.1:c.1658T= ENSP00000514619.1:p.Ile553=
ENST00000699819.1:c.*1220T= ENSP00000514620.1:n.*1220T=
ENST00000699820.1:c.*1T= ENSP00000514621.1:n.*1T=
ENST00000699821.1:c.1658T= ENSP00000514622.1:p.Ile553=
ENST00000699822.1:c.*1515T= ENSP00000514623.1:n.*1515T=
ENST00000699823.1:c.1658T= ENSP00000514624.1:p.Ile553=
ENST00000699824.1:c.*1566T= ENSP00000514625.1:n.*1566T=
ENST00000699825.1:c.1502T= ENSP00000514626.1:p.Ile501=
ENST00000699826.1:c.*1462T= ENSP00000514627.1:n.*1462T=
ENST00000699827.1:c.1895T= ENSP00000514628.1:p.Ile632=
ENST00000699828.1:c.*1153T= ENSP00000514629.1:n.*1153T=
ENST00000699833.1:n.3835T=
ENST00000699837.1:c.1658T= ENSP00000514635.1:p.Ile553=
ENST00000699838.1:c.*1963T= ENSP00000514636.1:n.*1963T=
ENST00000699839.1:c.2249T= ENSP00000514637.1:p.Ile750=
ENST00000699916.1:c.*1320T= ENSP00000514684.1:n.*1320T=
ENST00000699917.1:c.*1512T= ENSP00000514685.1:n.*1512T=
ENST00000699918.1:c.*1564T= ENSP00000514686.1:n.*1564T=
ENST00000699919.1:c.*1650T= ENSP00000514687.1:n.*1650T=
ENST00000699920.1:c.*1699T= ENSP00000514688.1:n.*1699T=
ENST00000699928.1:c.*1T= ENSP00000514693.1:n.*1T=
ENST00000699951.1:c.*1159T= ENSP00000514706.1:n.*1159T=
ENST00000699952.1:c.804-9393T= ENSP00000514707.1:n.804-9393T=
ENST00000265849.12:c.2063T= MANE Select ENSP00000265849.7:p.Ile688=
ENST00000642292.1:c.1658T= ENSP00000495524.1:p.Ile553=
ENST00000642456.1:c.1658T= ENSP00000493814.1:p.Ile553=
ENST00000643595.1:c.*1462T= ENSP00000494497.1:n.*1462T=
ENST00000644110.1:c.1745T= ENSP00000496392.1:p.Ile582=
ENST00000265849.11:c.2063T= ENSP00000265849.7:p.Ile688=
ENST00000382321.5:c.860T= ENSP00000371758.4:p.Ile287=
ENST00000406569.7:n.1678+4152T=
ENST00000441476.6:c.1745T= ENSP00000392843.2:p.Ile582=
ENST00000469652.1:n.63-30T=
NM_000535.5:c.2063T= , LRG_161t1:c.2063T= NP_000526.1:p.Ile688=
NR_003085.2:n.2145T=
XM_006715742.2:c.2057T= XP_006715805.1:p.Ile686=
XM_006715744.2:c.1130T= XP_006715807.1:p.Ile377=
XM_011515427.1:c.2108T= XP_011513729.1:p.Ile703=
XM_011515428.1:c.1952T= XP_011513730.1:p.Ile651=
XM_011515429.1:c.1745T= XP_011513731.1:p.Ile582=
XM_011515430.1:c.1745T= XP_011513732.1:p.Ile582=
NM_000535.6:c.2063T= NP_000526.2:p.Ile688=
NM_001322003.1:c.1658T= NP_001308932.1:p.Ile553=
NM_001322004.1:c.1658T= NP_001308933.1:p.Ile553=
NM_001322005.1:c.1658T= NP_001308934.1:p.Ile553=
NM_001322006.1:c.1907T= NP_001308935.1:p.Ile636=
NM_001322007.1:c.1745T= NP_001308936.1:p.Ile582=
NM_001322008.1:c.1745T= NP_001308937.1:p.Ile582=
NM_001322009.1:c.1658T= NP_001308938.1:p.Ile553=
NM_001322010.1:c.1502T= NP_001308939.1:p.Ile501=
NM_001322011.1:c.1130T= NP_001308940.1:p.Ile377=
NM_001322012.1:c.1130T= NP_001308941.1:p.Ile377=
NM_001322013.1:c.1490T= NP_001308942.1:p.Ile497=
NM_001322014.1:c.2063T= NP_001308943.1:p.Ile688=
NM_001322015.1:c.1754T= NP_001308944.1:p.Ile585=
NR_136154.1:n.2150T=
XM_006715744.4:c.1130T= XP_006715807.1:p.Ile377=
XM_017012342.2:c.1130T= XP_016867831.1:p.Ile377=
XM_024446800.1:c.1502T= XP_024302568.1:p.Ile501=
NM_000535.7:c.2063T= MANE Select NP_000526.2:p.Ile688=
NM_001322003.2:c.1658T= NP_001308932.1:p.Ile553=
NM_001322004.2:c.1658T= NP_001308933.1:p.Ile553=
NM_001322005.2:c.1658T= NP_001308934.1:p.Ile553=
NM_001322006.2:c.1907T= NP_001308935.1:p.Ile636=
NM_001322008.2:c.1745T= NP_001308937.1:p.Ile582=
NM_001322009.2:c.1658T= NP_001308938.1:p.Ile553=
NM_001322010.2:c.1502T= NP_001308939.1:p.Ile501=
NM_001322011.2:c.1130T= NP_001308940.1:p.Ile377=
NM_001322012.2:c.1130T= NP_001308941.1:p.Ile377=
NM_001322013.2:c.1490T= NP_001308942.1:p.Ile497=
NM_001322014.2:c.2063T= NP_001308943.1:p.Ile688=
NM_001322015.2:c.1754T= NP_001308944.1:p.Ile585=
NM_001322007.2:c.1745T= NP_001308936.1:p.Ile582=