Canonical Allele Identifier: CA1685230530
Gene: PMS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5987434C= , CM000669.2:g.5987434C= GRCh38
NC_000007.13:g.6027065C= , CM000669.1:g.6027065C= GRCh37
NC_000007.12:g.5993591C= NCBI36
NG_008466.1:g.26673G= , LRG_161:g.26673G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000699814.2:c.*727G= ENSP00000514615.2:n.*727G=
ENST00000699840.2:c.1328G= ENSP00000514638.2:p.Arg443=
ENST00000699930.2:c.1223G= ENSP00000514695.2:p.Arg408=
ENST00000406569.8:c.1331G= ENSP00000514464.1:p.Arg444=
ENST00000644110.2:c.*925G= ENSP00000496392.2:n.*925G=
ENST00000699752.1:c.1175G= ENSP00000514561.1:p.Arg392=
ENST00000699753.1:c.*752G= ENSP00000514562.1:n.*752G=
ENST00000699754.1:c.1133G= ENSP00000514563.1:p.Arg378=
ENST00000699755.1:c.*730G= ENSP00000514564.1:n.*730G=
ENST00000699756.1:c.*918G= ENSP00000514565.1:n.*918G=
ENST00000699757.1:c.*588G= ENSP00000514566.1:n.*588G=
ENST00000699758.1:c.*588G= ENSP00000514567.1:n.*588G=
ENST00000699759.1:n.2185G=
ENST00000699760.1:c.1013G= ENSP00000514568.1:p.Arg338=
ENST00000699761.1:c.926G= ENSP00000514569.1:p.Arg309=
ENST00000699762.1:c.758G= ENSP00000514570.1:p.Arg253=
ENST00000699763.1:c.*421G= ENSP00000514571.1:n.*421G=
ENST00000699764.1:c.1331G= ENSP00000514572.1:p.Arg444=
ENST00000699765.1:c.*427G= ENSP00000514573.1:n.*427G=
ENST00000699766.1:c.1331G= ENSP00000514574.1:p.Arg444=
ENST00000699767.1:c.1331G= ENSP00000514575.1:p.Arg444=
ENST00000699768.1:c.1331G= ENSP00000514576.1:p.Arg444=
ENST00000699811.1:c.926G= ENSP00000514614.1:p.Arg309=
ENST00000699813.1:n.1444G=
ENST00000699814.1:c.954G=
ENST00000699815.1:c.*862G= ENSP00000514616.1:n.*862G=
ENST00000699816.1:c.*221G= ENSP00000514617.1:n.*221G=
ENST00000699817.1:c.*925G= ENSP00000514618.1:n.*925G=
ENST00000699818.1:c.926G= ENSP00000514619.1:p.Arg309=
ENST00000699819.1:c.*488G= ENSP00000514620.1:n.*488G=
ENST00000699820.1:c.1144+2366G= ENSP00000514621.1:n.1144+2366G=
ENST00000699821.1:c.926G= ENSP00000514622.1:p.Arg309=
ENST00000699822.1:c.*783G= ENSP00000514623.1:n.*783G=
ENST00000699823.1:c.926G= ENSP00000514624.1:p.Arg309=
ENST00000699824.1:c.*834G= ENSP00000514625.1:n.*834G=
ENST00000699825.1:c.770G= ENSP00000514626.1:p.Arg257=
ENST00000699826.1:c.*730G= ENSP00000514627.1:n.*730G=
ENST00000699827.1:c.1163G= ENSP00000514628.1:p.Arg388=
ENST00000699828.1:c.*421G= ENSP00000514629.1:n.*421G=
ENST00000699833.1:n.3103G=
ENST00000699837.1:c.926G= ENSP00000514635.1:p.Arg309=
ENST00000699838.1:c.*1231G= ENSP00000514636.1:n.*1231G=
ENST00000699839.1:c.1517G= ENSP00000514637.1:p.Arg506=
ENST00000699916.1:c.*588G= ENSP00000514684.1:n.*588G=
ENST00000699917.1:c.*780G= ENSP00000514685.1:n.*780G=
ENST00000699918.1:c.*832G= ENSP00000514686.1:n.*832G=
ENST00000699919.1:c.*918G= ENSP00000514687.1:n.*918G=
ENST00000699920.1:c.*967G= ENSP00000514688.1:n.*967G=
ENST00000699928.1:c.989-4443G= ENSP00000514693.1:n.989-4443G=
ENST00000699929.1:c.*632G= ENSP00000514694.1:n.*632G=
ENST00000699930.1:c.1223G= ENSP00000514695.1:p.Arg408=
ENST00000699931.1:n.2759G=
ENST00000699951.1:c.*427G= ENSP00000514706.1:n.*427G=
ENST00000699952.1:c.803+9892G= ENSP00000514707.1:n.803+9892G=
ENST00000699953.1:c.*438G= ENSP00000514708.1:n.*438G=
ENST00000699954.1:c.*632G= ENSP00000514709.1:n.*632G=
ENST00000265849.12:c.1331G= MANE Select ENSP00000265849.7:p.Arg444=
ENST00000642292.1:c.926G= ENSP00000495524.1:p.Arg309=
ENST00000642456.1:c.926G= ENSP00000493814.1:p.Arg309=
ENST00000643595.1:c.*730G= ENSP00000494497.1:n.*730G=
ENST00000644110.1:c.1013G= ENSP00000496392.1:p.Arg338=
ENST00000265849.11:c.1331G= ENSP00000265849.7:p.Arg444=
ENST00000382321.5:c.804-4443G= ENSP00000371758.4:n.804-4443G=
ENST00000406569.7:n.1331G=
ENST00000441476.6:c.1013G= ENSP00000392843.2:p.Arg338=
ENST00000469652.1:n.63-4529G=
NM_000535.5:c.1331G= , LRG_161t1:c.1331G= NP_000526.1:p.Arg444=
NR_003085.2:n.1413G=
XM_006715742.2:c.1325G= XP_006715805.1:p.Arg442=
XM_006715744.2:c.398G= XP_006715807.1:p.Arg133=
XM_011515427.1:c.1376G= XP_011513729.1:p.Arg459=
XM_011515428.1:c.1220G= XP_011513730.1:p.Arg407=
XM_011515429.1:c.1013G= XP_011513731.1:p.Arg338=
XM_011515430.1:c.1013G= XP_011513732.1:p.Arg338=
NM_000535.6:c.1331G= NP_000526.2:p.Arg444=
NM_001322003.1:c.926G= NP_001308932.1:p.Arg309=
NM_001322004.1:c.926G= NP_001308933.1:p.Arg309=
NM_001322005.1:c.926G= NP_001308934.1:p.Arg309=
NM_001322006.1:c.1175G= NP_001308935.1:p.Arg392=
NM_001322007.1:c.1013G= NP_001308936.1:p.Arg338=
NM_001322008.1:c.1013G= NP_001308937.1:p.Arg338=
NM_001322009.1:c.926G= NP_001308938.1:p.Arg309=
NM_001322010.1:c.770G= NP_001308939.1:p.Arg257=
NM_001322011.1:c.398G= NP_001308940.1:p.Arg133=
NM_001322012.1:c.398G= NP_001308941.1:p.Arg133=
NM_001322013.1:c.758G= NP_001308942.1:p.Arg253=
NM_001322014.1:c.1331G= NP_001308943.1:p.Arg444=
NM_001322015.1:c.1022G= NP_001308944.1:p.Arg341=
NR_136154.1:n.1418G=
XM_006715744.4:c.398G= XP_006715807.1:p.Arg133=
XM_017012342.2:c.398G= XP_016867831.1:p.Arg133=
XM_024446800.1:c.770G= XP_024302568.1:p.Arg257=
NM_000535.7:c.1331G= MANE Select NP_000526.2:p.Arg444=
NM_001322003.2:c.926G= NP_001308932.1:p.Arg309=
NM_001322004.2:c.926G= NP_001308933.1:p.Arg309=
NM_001322005.2:c.926G= NP_001308934.1:p.Arg309=
NM_001322006.2:c.1175G= NP_001308935.1:p.Arg392=
NM_001322008.2:c.1013G= NP_001308937.1:p.Arg338=
NM_001322009.2:c.926G= NP_001308938.1:p.Arg309=
NM_001322010.2:c.770G= NP_001308939.1:p.Arg257=
NM_001322011.2:c.398G= NP_001308940.1:p.Arg133=
NM_001322012.2:c.398G= NP_001308941.1:p.Arg133=
NM_001322013.2:c.758G= NP_001308942.1:p.Arg253=
NM_001322014.2:c.1331G= NP_001308943.1:p.Arg444=
NM_001322015.2:c.1022G= NP_001308944.1:p.Arg341=
NM_001322007.2:c.1013G= NP_001308936.1:p.Arg338=