Canonical Allele Identifier: CA1286884432

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428368C= , CM000664.2:g.127428368C=	GRCh38
NC_000002.11:g.128185944C= , CM000664.1:g.128185944C=	GRCh37
NC_000002.10:g.127902414C=	NCBI36
NG_016323.1:g.14949C= , LRG_599:g.14949C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.808C= MANE Select	ENSP00000234071.4:p.Leu270=
ENST00000234071.7:c.808C=	ENSP00000234071.3:p.Leu270=
ENST00000402125.2:c.132C=
ENST00000409048.1:c.910C=	ENSP00000386679.1:p.Leu304=
NM_000312.3:c.808C= , LRG_599t1:c.808C=	NP_000303.1:p.Leu270=
XM_005263715.3:c.991C=	XP_005263772.1:p.Leu331=
XM_005263716.3:c.973C=	XP_005263773.1:p.Leu325=
XM_005263717.3:c.871C=	XP_005263774.1:p.Leu291=
XR_923313.1:n.1332-104G=
XM_005263717.4:c.871C=	XP_005263774.1:p.Leu291=
XM_017004505.1:c.1051C=	XP_016859994.1:p.Leu351=
XM_024453002.1:c.1153C=	XP_024308770.1:p.Leu385=
XM_024453003.1:c.1093C=	XP_024308771.1:p.Leu365=
XM_024453004.1:c.991C=	XP_024308772.1:p.Leu331=
XM_024453005.1:c.973C=	XP_024308773.1:p.Leu325=
XM_024453006.1:c.910C=	XP_024308774.1:p.Leu304=
XR_001739705.1:n.3607-104G=
XR_923313.2:n.4043-104G=
NM_000312.4:c.808C= MANE Select	NP_000303.1:p.Leu270=
NM_001375602.1:c.991C=	NP_001362531.1:p.Leu331=
NM_001375603.1:c.973C=	NP_001362532.1:p.Leu325=
NM_001375604.1:c.871C=	NP_001362533.1:p.Leu291=
NM_001375605.1:c.910C=	NP_001362534.1:p.Leu304=
NM_001375606.1:c.976C=	NP_001362535.1:p.Leu326=
NM_001375607.1:c.994C=	NP_001362536.1:p.Leu332=
NM_001375608.1:c.751C=	NP_001362537.1:p.Leu251=
NM_001375609.1:c.784C=	NP_001362538.1:p.Leu262=
NM_001375610.1:c.802C=	NP_001362539.1:p.Leu268=
NM_001375611.1:c.808C=	NP_001362540.1:p.Leu270=
NM_001375613.1:c.808C=	NP_001362542.1:p.Leu270=