Canonical Allele Identifier: CA1685217974
Gene: PMS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5982991A= , CM000669.2:g.5982991A= GRCh38
NC_000007.13:g.6022622A= , CM000669.1:g.6022622A= GRCh37
NC_000007.12:g.5989148A= NCBI36
NG_008466.1:g.31116T= , LRG_161:g.31116T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000699814.2:c.*1403T= ENSP00000514615.2:n.*1403T=
ENST00000699840.2:c.2004T= ENSP00000514638.2:p.Ser668=
ENST00000699930.2:c.1899T= ENSP00000514695.2:p.Ser633=
ENST00000406569.8:c.1678+4096T= ENSP00000514464.1:n.1678+4096T=
ENST00000644110.2:c.*1601T= ENSP00000496392.2:n.*1601T=
ENST00000699752.1:c.1851T= ENSP00000514561.1:p.Ser617=
ENST00000699753.1:c.*1428T= ENSP00000514562.1:n.*1428T=
ENST00000699754.1:c.1809T= ENSP00000514563.1:p.Ser603=
ENST00000699755.1:c.*1406T= ENSP00000514564.1:n.*1406T=
ENST00000699756.1:c.*1594T= ENSP00000514565.1:n.*1594T=
ENST00000699757.1:c.*1264T= ENSP00000514566.1:n.*1264T=
ENST00000699758.1:c.*1264T= ENSP00000514567.1:n.*1264T=
ENST00000699759.1:n.2861T=
ENST00000699760.1:c.1689T= ENSP00000514568.1:p.Ser563=
ENST00000699761.1:c.1602T= ENSP00000514569.1:p.Ser534=
ENST00000699762.1:c.1434T= ENSP00000514570.1:p.Ser478=
ENST00000699763.1:c.*1097T= ENSP00000514571.1:n.*1097T=
ENST00000699764.1:c.*325T= ENSP00000514572.1:n.*325T=
ENST00000699765.1:c.*1103T= ENSP00000514573.1:n.*1103T=
ENST00000699766.1:c.2007T= ENSP00000514574.1:p.Ser669=
ENST00000699767.1:c.2007T= ENSP00000514575.1:p.Ser669=
ENST00000699768.1:c.2007T= ENSP00000514576.1:p.Ser669=
ENST00000699811.1:c.1602T= ENSP00000514614.1:p.Ser534=
ENST00000699813.1:n.2120T=
ENST00000699814.1:c.1630T=
ENST00000699815.1:c.*1538T= ENSP00000514616.1:n.*1538T=
ENST00000699816.1:c.*897T= ENSP00000514617.1:n.*897T=
ENST00000699817.1:c.*1601T= ENSP00000514618.1:n.*1601T=
ENST00000699818.1:c.1602T= ENSP00000514619.1:p.Ser534=
ENST00000699819.1:c.*1164T= ENSP00000514620.1:n.*1164T=
ENST00000699820.1:c.1145T= ENSP00000514621.1:p.Val382=
ENST00000699821.1:c.1602T= ENSP00000514622.1:p.Ser534=
ENST00000699822.1:c.*1459T= ENSP00000514623.1:n.*1459T=
ENST00000699823.1:c.1602T= ENSP00000514624.1:p.Ser534=
ENST00000699824.1:c.*1510T= ENSP00000514625.1:n.*1510T=
ENST00000699825.1:c.1446T= ENSP00000514626.1:p.Ser482=
ENST00000699826.1:c.*1406T= ENSP00000514627.1:n.*1406T=
ENST00000699827.1:c.1839T= ENSP00000514628.1:p.Ser613=
ENST00000699828.1:c.*1097T= ENSP00000514629.1:n.*1097T=
ENST00000699833.1:n.3779T=
ENST00000699837.1:c.1602T= ENSP00000514635.1:p.Ser534=
ENST00000699838.1:c.*1907T= ENSP00000514636.1:n.*1907T=
ENST00000699839.1:c.2193T= ENSP00000514637.1:p.Ser731=
ENST00000699916.1:c.*1264T= ENSP00000514684.1:n.*1264T=
ENST00000699917.1:c.*1456T= ENSP00000514685.1:n.*1456T=
ENST00000699918.1:c.*1508T= ENSP00000514686.1:n.*1508T=
ENST00000699919.1:c.*1594T= ENSP00000514687.1:n.*1594T=
ENST00000699920.1:c.*1643T= ENSP00000514688.1:n.*1643T=
ENST00000699928.1:c.989T= ENSP00000514693.1:p.Val330=
ENST00000699951.1:c.*1103T= ENSP00000514706.1:n.*1103T=
ENST00000699952.1:c.804-9449T= ENSP00000514707.1:n.804-9449T=
ENST00000265849.12:c.2007T= MANE Select ENSP00000265849.7:p.Ser669=
ENST00000642292.1:c.1602T= ENSP00000495524.1:p.Ser534=
ENST00000642456.1:c.1602T= ENSP00000493814.1:p.Ser534=
ENST00000643595.1:c.*1406T= ENSP00000494497.1:n.*1406T=
ENST00000644110.1:c.1689T= ENSP00000496392.1:p.Ser563=
ENST00000265849.11:c.2007T= ENSP00000265849.7:p.Ser669=
ENST00000382321.5:c.804T= ENSP00000371758.4:p.Tyr268=
ENST00000406569.7:n.1678+4096T=
ENST00000441476.6:c.1689T= ENSP00000392843.2:p.Ser563=
ENST00000469652.1:n.63-86T=
NM_000535.5:c.2007T= , LRG_161t1:c.2007T= NP_000526.1:p.Ser669=
NR_003085.2:n.2089T=
XM_006715742.2:c.2001T= XP_006715805.1:p.Ser667=
XM_006715744.2:c.1074T= XP_006715807.1:p.Ser358=
XM_011515427.1:c.2052T= XP_011513729.1:p.Ser684=
XM_011515428.1:c.1896T= XP_011513730.1:p.Ser632=
XM_011515429.1:c.1689T= XP_011513731.1:p.Ser563=
XM_011515430.1:c.1689T= XP_011513732.1:p.Ser563=
NM_000535.6:c.2007T= NP_000526.2:p.Ser669=
NM_001322003.1:c.1602T= NP_001308932.1:p.Ser534=
NM_001322004.1:c.1602T= NP_001308933.1:p.Ser534=
NM_001322005.1:c.1602T= NP_001308934.1:p.Ser534=
NM_001322006.1:c.1851T= NP_001308935.1:p.Ser617=
NM_001322007.1:c.1689T= NP_001308936.1:p.Ser563=
NM_001322008.1:c.1689T= NP_001308937.1:p.Ser563=
NM_001322009.1:c.1602T= NP_001308938.1:p.Ser534=
NM_001322010.1:c.1446T= NP_001308939.1:p.Ser482=
NM_001322011.1:c.1074T= NP_001308940.1:p.Ser358=
NM_001322012.1:c.1074T= NP_001308941.1:p.Ser358=
NM_001322013.1:c.1434T= NP_001308942.1:p.Ser478=
NM_001322014.1:c.2007T= NP_001308943.1:p.Ser669=
NM_001322015.1:c.1698T= NP_001308944.1:p.Ser566=
NR_136154.1:n.2094T=
XM_006715744.4:c.1074T= XP_006715807.1:p.Ser358=
XM_017012342.2:c.1074T= XP_016867831.1:p.Ser358=
XM_024446800.1:c.1446T= XP_024302568.1:p.Ser482=
NM_000535.7:c.2007T= MANE Select NP_000526.2:p.Ser669=
NM_001322003.2:c.1602T= NP_001308932.1:p.Ser534=
NM_001322004.2:c.1602T= NP_001308933.1:p.Ser534=
NM_001322005.2:c.1602T= NP_001308934.1:p.Ser534=
NM_001322006.2:c.1851T= NP_001308935.1:p.Ser617=
NM_001322008.2:c.1689T= NP_001308937.1:p.Ser563=
NM_001322009.2:c.1602T= NP_001308938.1:p.Ser534=
NM_001322010.2:c.1446T= NP_001308939.1:p.Ser482=
NM_001322011.2:c.1074T= NP_001308940.1:p.Ser358=
NM_001322012.2:c.1074T= NP_001308941.1:p.Ser358=
NM_001322013.2:c.1434T= NP_001308942.1:p.Ser478=
NM_001322014.2:c.2007T= NP_001308943.1:p.Ser669=
NM_001322015.2:c.1698T= NP_001308944.1:p.Ser566=
NM_001322007.2:c.1689T= NP_001308936.1:p.Ser563=