Canonical Allele Identifier: CA1286884661

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428803T= , CM000664.2:g.127428803T=	GRCh38
NC_000002.11:g.128186379T= , CM000664.1:g.128186379T=	GRCh37
NC_000002.10:g.127902849T=	NCBI36
NG_016323.1:g.15384T= , LRG_599:g.15384T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.1243T= MANE Select	ENSP00000234071.4:p.Phe415=
ENST00000234071.7:c.1243T=	ENSP00000234071.3:p.Phe415=
ENST00000402125.2:c.567T=
ENST00000409048.1:c.1345T=	ENSP00000386679.1:p.Phe449=
NM_000312.3:c.1243T= , LRG_599t1:c.1243T=	NP_000303.1:p.Phe415=
XM_005263715.3:c.1426T=	XP_005263772.1:p.Phe476=
XM_005263716.3:c.1408T=	XP_005263773.1:p.Phe470=
XM_005263717.3:c.1306T=	XP_005263774.1:p.Phe436=
XR_923313.1:n.1332-539A=
XM_005263717.4:c.1306T=	XP_005263774.1:p.Phe436=
XM_017004505.1:c.1486T=	XP_016859994.1:p.Phe496=
XM_024453002.1:c.1588T=	XP_024308770.1:p.Phe530=
XM_024453003.1:c.1528T=	XP_024308771.1:p.Phe510=
XM_024453004.1:c.1426T=	XP_024308772.1:p.Phe476=
XM_024453005.1:c.1408T=	XP_024308773.1:p.Phe470=
XM_024453006.1:c.1345T=	XP_024308774.1:p.Phe449=
XR_001739705.1:n.3607-539A=
XR_923313.2:n.4043-539A=
NM_000312.4:c.1243T= MANE Select	NP_000303.1:p.Phe415=
NM_001375602.1:c.1426T=	NP_001362531.1:p.Phe476=
NM_001375603.1:c.1408T=	NP_001362532.1:p.Phe470=
NM_001375604.1:c.1306T=	NP_001362533.1:p.Phe436=
NM_001375605.1:c.1345T=	NP_001362534.1:p.Phe449=
NM_001375606.1:c.1411T=	NP_001362535.1:p.Phe471=
NM_001375607.1:c.1429T=	NP_001362536.1:p.Phe477=
NM_001375608.1:c.1186T=	NP_001362537.1:p.Phe396=
NM_001375609.1:c.1219T=	NP_001362538.1:p.Phe407=
NM_001375610.1:c.1237T=	NP_001362539.1:p.Phe413=
NM_001375611.1:c.1243T=	NP_001362540.1:p.Phe415=
NM_001375613.1:c.1243T=	NP_001362542.1:p.Phe415=