Canonical Allele Identifier: CA1286884712

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428904C= , CM000664.2:g.127428904C=	GRCh38
NC_000002.11:g.128186480C= , CM000664.1:g.128186480C=	GRCh37
NC_000002.10:g.127902950C=	NCBI36
NG_016323.1:g.15485C= , LRG_599:g.15485C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.1344C= MANE Select	ENSP00000234071.4:p.His448=
ENST00000234071.7:c.1344C=	ENSP00000234071.3:p.His448=
ENST00000402125.2:c.668C=
ENST00000409048.1:c.1446C=	ENSP00000386679.1:p.His482=
NM_000312.3:c.1344C= , LRG_599t1:c.1344C=	NP_000303.1:p.His448=
XM_005263715.3:c.1527C=	XP_005263772.1:p.His509=
XM_005263716.3:c.1509C=	XP_005263773.1:p.His503=
XM_005263717.3:c.1407C=	XP_005263774.1:p.His469=
XR_923313.1:n.1332-640G=
XM_005263717.4:c.1407C=	XP_005263774.1:p.His469=
XM_017004505.1:c.1587C=	XP_016859994.1:p.His529=
XM_024453002.1:c.1689C=	XP_024308770.1:p.His563=
XM_024453003.1:c.1629C=	XP_024308771.1:p.His543=
XM_024453004.1:c.1527C=	XP_024308772.1:p.His509=
XM_024453005.1:c.1509C=	XP_024308773.1:p.His503=
XM_024453006.1:c.1446C=	XP_024308774.1:p.His482=
XR_001739705.1:n.3607-640G=
XR_923313.2:n.4043-640G=
NM_000312.4:c.1344C= MANE Select	NP_000303.1:p.His448=
NM_001375602.1:c.1527C=	NP_001362531.1:p.His509=
NM_001375603.1:c.1509C=	NP_001362532.1:p.His503=
NM_001375604.1:c.1407C=	NP_001362533.1:p.His469=
NM_001375605.1:c.1446C=	NP_001362534.1:p.His482=
NM_001375606.1:c.1512C=	NP_001362535.1:p.His504=
NM_001375607.1:c.1530C=	NP_001362536.1:p.His510=
NM_001375608.1:c.1287C=	NP_001362537.1:p.His429=
NM_001375609.1:c.1320C=	NP_001362538.1:p.His440=
NM_001375610.1:c.1338C=	NP_001362539.1:p.His446=
NM_001375611.1:c.1344C=	NP_001362540.1:p.His448=
NM_001375613.1:c.1344C=	NP_001362542.1:p.His448=