Canonical Allele Identifier: CA1286884636

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428761G= , CM000664.2:g.127428761G=	GRCh38
NC_000002.11:g.128186337G= , CM000664.1:g.128186337G=	GRCh37
NC_000002.10:g.127902807G=	NCBI36
NG_016323.1:g.15342G= , LRG_599:g.15342G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.1201G= MANE Select	ENSP00000234071.4:p.Asp401=
ENST00000234071.7:c.1201G=	ENSP00000234071.3:p.Asp401=
ENST00000402125.2:c.525G=
ENST00000409048.1:c.1303G=	ENSP00000386679.1:p.Asp435=
NM_000312.3:c.1201G= , LRG_599t1:c.1201G=	NP_000303.1:p.Asp401=
XM_005263715.3:c.1384G=	XP_005263772.1:p.Asp462=
XM_005263716.3:c.1366G=	XP_005263773.1:p.Asp456=
XM_005263717.3:c.1264G=	XP_005263774.1:p.Asp422=
XR_923313.1:n.1332-497C=
XM_005263717.4:c.1264G=	XP_005263774.1:p.Asp422=
XM_017004505.1:c.1444G=	XP_016859994.1:p.Asp482=
XM_024453002.1:c.1546G=	XP_024308770.1:p.Asp516=
XM_024453003.1:c.1486G=	XP_024308771.1:p.Asp496=
XM_024453004.1:c.1384G=	XP_024308772.1:p.Asp462=
XM_024453005.1:c.1366G=	XP_024308773.1:p.Asp456=
XM_024453006.1:c.1303G=	XP_024308774.1:p.Asp435=
XR_001739705.1:n.3607-497C=
XR_923313.2:n.4043-497C=
NM_000312.4:c.1201G= MANE Select	NP_000303.1:p.Asp401=
NM_001375602.1:c.1384G=	NP_001362531.1:p.Asp462=
NM_001375603.1:c.1366G=	NP_001362532.1:p.Asp456=
NM_001375604.1:c.1264G=	NP_001362533.1:p.Asp422=
NM_001375605.1:c.1303G=	NP_001362534.1:p.Asp435=
NM_001375606.1:c.1369G=	NP_001362535.1:p.Asp457=
NM_001375607.1:c.1387G=	NP_001362536.1:p.Asp463=
NM_001375608.1:c.1144G=	NP_001362537.1:p.Asp382=
NM_001375609.1:c.1177G=	NP_001362538.1:p.Asp393=
NM_001375610.1:c.1195G=	NP_001362539.1:p.Asp399=
NM_001375611.1:c.1201G=	NP_001362540.1:p.Asp401=
NM_001375613.1:c.1201G=	NP_001362542.1:p.Asp401=