Canonical Allele Identifier: CA1286884461

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428425C= , CM000664.2:g.127428425C=	GRCh38
NC_000002.11:g.128186001C= , CM000664.1:g.128186001C=	GRCh37
NC_000002.10:g.127902471C=	NCBI36
NG_016323.1:g.15006C= , LRG_599:g.15006C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.865C= MANE Select	ENSP00000234071.4:p.Pro289=
ENST00000234071.7:c.865C=	ENSP00000234071.3:p.Pro289=
ENST00000402125.2:c.189C=
ENST00000409048.1:c.967C=	ENSP00000386679.1:p.Pro323=
NM_000312.3:c.865C= , LRG_599t1:c.865C=	NP_000303.1:p.Pro289=
XM_005263715.3:c.1048C=	XP_005263772.1:p.Pro350=
XM_005263716.3:c.1030C=	XP_005263773.1:p.Pro344=
XM_005263717.3:c.928C=	XP_005263774.1:p.Pro310=
XR_923313.1:n.1332-161G=
XM_005263717.4:c.928C=	XP_005263774.1:p.Pro310=
XM_017004505.1:c.1108C=	XP_016859994.1:p.Pro370=
XM_024453002.1:c.1210C=	XP_024308770.1:p.Pro404=
XM_024453003.1:c.1150C=	XP_024308771.1:p.Pro384=
XM_024453004.1:c.1048C=	XP_024308772.1:p.Pro350=
XM_024453005.1:c.1030C=	XP_024308773.1:p.Pro344=
XM_024453006.1:c.967C=	XP_024308774.1:p.Pro323=
XR_001739705.1:n.3607-161G=
XR_923313.2:n.4043-161G=
NM_000312.4:c.865C= MANE Select	NP_000303.1:p.Pro289=
NM_001375602.1:c.1048C=	NP_001362531.1:p.Pro350=
NM_001375603.1:c.1030C=	NP_001362532.1:p.Pro344=
NM_001375604.1:c.928C=	NP_001362533.1:p.Pro310=
NM_001375605.1:c.967C=	NP_001362534.1:p.Pro323=
NM_001375606.1:c.1033C=	NP_001362535.1:p.Pro345=
NM_001375607.1:c.1051C=	NP_001362536.1:p.Pro351=
NM_001375608.1:c.808C=	NP_001362537.1:p.Pro270=
NM_001375609.1:c.841C=	NP_001362538.1:p.Pro281=
NM_001375610.1:c.859C=	NP_001362539.1:p.Pro287=
NM_001375611.1:c.865C=	NP_001362540.1:p.Pro289=
NM_001375613.1:c.865C=	NP_001362542.1:p.Pro289=