Canonical Allele Identifier: CA1685217615

Gene: PMS2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5982919C= , CM000669.2:g.5982919C=	GRCh38
NC_000007.13:g.6022550C= , CM000669.1:g.6022550C=	GRCh37
NC_000007.12:g.5989076C=	NCBI36
NG_008466.1:g.31188G= , LRG_161:g.31188G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699814.2:c.*1475G=	ENSP00000514615.2:n.*1475G=
ENST00000699840.2:c.2076G=	ENSP00000514638.2:p.Glu692=
ENST00000699930.2:c.1971G=	ENSP00000514695.2:p.Glu657=
ENST00000406569.8:c.1678+4168G=	ENSP00000514464.1:n.1678+4168G=
ENST00000644110.2:c.*1673G=	ENSP00000496392.2:n.*1673G=
ENST00000699752.1:c.1923G=	ENSP00000514561.1:p.Glu641=
ENST00000699753.1:c.*1500G=	ENSP00000514562.1:n.*1500G=
ENST00000699754.1:c.1881G=	ENSP00000514563.1:p.Glu627=
ENST00000699755.1:c.*1478G=	ENSP00000514564.1:n.*1478G=
ENST00000699756.1:c.*1666G=	ENSP00000514565.1:n.*1666G=
ENST00000699757.1:c.*1336G=	ENSP00000514566.1:n.*1336G=
ENST00000699758.1:c.*1336G=	ENSP00000514567.1:n.*1336G=
ENST00000699759.1:n.2933G=
ENST00000699760.1:c.1761G=	ENSP00000514568.1:p.Glu587=
ENST00000699761.1:c.1674G=	ENSP00000514569.1:p.Glu558=
ENST00000699762.1:c.1506G=	ENSP00000514570.1:p.Glu502=
ENST00000699763.1:c.*1169G=	ENSP00000514571.1:n.*1169G=
ENST00000699764.1:c.*397G=	ENSP00000514572.1:n.*397G=
ENST00000699765.1:c.*1175G=	ENSP00000514573.1:n.*1175G=
ENST00000699766.1:c.2079G=	ENSP00000514574.1:p.Glu693=
ENST00000699767.1:c.2079G=	ENSP00000514575.1:p.Glu693=
ENST00000699768.1:c.2079G=	ENSP00000514576.1:p.Glu693=
ENST00000699811.1:c.1674G=	ENSP00000514614.1:p.Glu558=
ENST00000699813.1:n.2192G=
ENST00000699814.1:c.1702G=
ENST00000699815.1:c.*1610G=	ENSP00000514616.1:n.*1610G=
ENST00000699816.1:c.*969G=	ENSP00000514617.1:n.*969G=
ENST00000699817.1:c.*1673G=	ENSP00000514618.1:n.*1673G=
ENST00000699818.1:c.1674G=	ENSP00000514619.1:p.Glu558=
ENST00000699819.1:c.*1236G=	ENSP00000514620.1:n.*1236G=
ENST00000699820.1:c.*17G=	ENSP00000514621.1:n.*17G=
ENST00000699821.1:c.1674G=	ENSP00000514622.1:p.Glu558=
ENST00000699822.1:c.*1531G=	ENSP00000514623.1:n.*1531G=
ENST00000699823.1:c.1674G=	ENSP00000514624.1:p.Glu558=
ENST00000699824.1:c.*1582G=	ENSP00000514625.1:n.*1582G=
ENST00000699825.1:c.1518G=	ENSP00000514626.1:p.Glu506=
ENST00000699826.1:c.*1478G=	ENSP00000514627.1:n.*1478G=
ENST00000699827.1:c.1911G=	ENSP00000514628.1:p.Glu637=
ENST00000699828.1:c.*1169G=	ENSP00000514629.1:n.*1169G=
ENST00000699833.1:n.3851G=
ENST00000699837.1:c.1674G=	ENSP00000514635.1:p.Glu558=
ENST00000699838.1:c.*1979G=	ENSP00000514636.1:n.*1979G=
ENST00000699839.1:c.2265G=	ENSP00000514637.1:p.Glu755=
ENST00000699916.1:c.*1336G=	ENSP00000514684.1:n.*1336G=
ENST00000699917.1:c.*1528G=	ENSP00000514685.1:n.*1528G=
ENST00000699918.1:c.*1580G=	ENSP00000514686.1:n.*1580G=
ENST00000699919.1:c.*1666G=	ENSP00000514687.1:n.*1666G=
ENST00000699920.1:c.*1715G=	ENSP00000514688.1:n.*1715G=
ENST00000699928.1:c.*17G=	ENSP00000514693.1:n.*17G=
ENST00000699951.1:c.*1175G=	ENSP00000514706.1:n.*1175G=
ENST00000699952.1:c.804-9377G=	ENSP00000514707.1:n.804-9377G=
ENST00000265849.12:c.2079G= MANE Select	ENSP00000265849.7:p.Glu693=
ENST00000642292.1:c.1674G=	ENSP00000495524.1:p.Glu558=
ENST00000642456.1:c.1674G=	ENSP00000493814.1:p.Glu558=
ENST00000643595.1:c.*1478G=	ENSP00000494497.1:n.*1478G=
ENST00000644110.1:c.1761G=	ENSP00000496392.1:p.Glu587=
ENST00000265849.11:c.2079G=	ENSP00000265849.7:p.Glu693=
ENST00000382321.5:c.876G=	ENSP00000371758.4:p.Glu292=
ENST00000406569.7:n.1678+4168G=
ENST00000441476.6:c.1761G=	ENSP00000392843.2:p.Glu587=
ENST00000469652.1:n.63-14G=
NM_000535.5:c.2079G= , LRG_161t1:c.2079G=	NP_000526.1:p.Glu693=
NR_003085.2:n.2161G=
XM_006715742.2:c.2073G=	XP_006715805.1:p.Glu691=
XM_006715744.2:c.1146G=	XP_006715807.1:p.Glu382=
XM_011515427.1:c.2124G=	XP_011513729.1:p.Glu708=
XM_011515428.1:c.1968G=	XP_011513730.1:p.Glu656=
XM_011515429.1:c.1761G=	XP_011513731.1:p.Glu587=
XM_011515430.1:c.1761G=	XP_011513732.1:p.Glu587=
NM_000535.6:c.2079G=	NP_000526.2:p.Glu693=
NM_001322003.1:c.1674G=	NP_001308932.1:p.Glu558=
NM_001322004.1:c.1674G=	NP_001308933.1:p.Glu558=
NM_001322005.1:c.1674G=	NP_001308934.1:p.Glu558=
NM_001322006.1:c.1923G=	NP_001308935.1:p.Glu641=
NM_001322007.1:c.1761G=	NP_001308936.1:p.Glu587=
NM_001322008.1:c.1761G=	NP_001308937.1:p.Glu587=
NM_001322009.1:c.1674G=	NP_001308938.1:p.Glu558=
NM_001322010.1:c.1518G=	NP_001308939.1:p.Glu506=
NM_001322011.1:c.1146G=	NP_001308940.1:p.Glu382=
NM_001322012.1:c.1146G=	NP_001308941.1:p.Glu382=
NM_001322013.1:c.1506G=	NP_001308942.1:p.Glu502=
NM_001322014.1:c.2079G=	NP_001308943.1:p.Glu693=
NM_001322015.1:c.1770G=	NP_001308944.1:p.Glu590=
NR_136154.1:n.2166G=
XM_006715744.4:c.1146G=	XP_006715807.1:p.Glu382=
XM_017012342.2:c.1146G=	XP_016867831.1:p.Glu382=
XM_024446800.1:c.1518G=	XP_024302568.1:p.Glu506=
NM_000535.7:c.2079G= MANE Select	NP_000526.2:p.Glu693=
NM_001322003.2:c.1674G=	NP_001308932.1:p.Glu558=
NM_001322004.2:c.1674G=	NP_001308933.1:p.Glu558=
NM_001322005.2:c.1674G=	NP_001308934.1:p.Glu558=
NM_001322006.2:c.1923G=	NP_001308935.1:p.Glu641=
NM_001322008.2:c.1761G=	NP_001308937.1:p.Glu587=
NM_001322009.2:c.1674G=	NP_001308938.1:p.Glu558=
NM_001322010.2:c.1518G=	NP_001308939.1:p.Glu506=
NM_001322011.2:c.1146G=	NP_001308940.1:p.Glu382=
NM_001322012.2:c.1146G=	NP_001308941.1:p.Glu382=
NM_001322013.2:c.1506G=	NP_001308942.1:p.Glu502=
NM_001322014.2:c.2079G=	NP_001308943.1:p.Glu693=
NM_001322015.2:c.1770G=	NP_001308944.1:p.Glu590=
NM_001322007.2:c.1761G=	NP_001308936.1:p.Glu587=