Canonical Allele Identifier: CA1286884526

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428559C= , CM000664.2:g.127428559C=	GRCh38
NC_000002.11:g.128186135C= , CM000664.1:g.128186135C=	GRCh37
NC_000002.10:g.127902605C=	NCBI36
NG_016323.1:g.15140C= , LRG_599:g.15140C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.999C= MANE Select	ENSP00000234071.4:p.Ala333=
ENST00000234071.7:c.999C=	ENSP00000234071.3:p.Ala333=
ENST00000402125.2:c.323C=
ENST00000409048.1:c.1101C=	ENSP00000386679.1:p.Ala367=
NM_000312.3:c.999C= , LRG_599t1:c.999C=	NP_000303.1:p.Ala333=
XM_005263715.3:c.1182C=	XP_005263772.1:p.Ala394=
XM_005263716.3:c.1164C=	XP_005263773.1:p.Ala388=
XM_005263717.3:c.1062C=	XP_005263774.1:p.Ala354=
XR_923313.1:n.1332-295G=
XM_005263717.4:c.1062C=	XP_005263774.1:p.Ala354=
XM_017004505.1:c.1242C=	XP_016859994.1:p.Ala414=
XM_024453002.1:c.1344C=	XP_024308770.1:p.Ala448=
XM_024453003.1:c.1284C=	XP_024308771.1:p.Ala428=
XM_024453004.1:c.1182C=	XP_024308772.1:p.Ala394=
XM_024453005.1:c.1164C=	XP_024308773.1:p.Ala388=
XM_024453006.1:c.1101C=	XP_024308774.1:p.Ala367=
XR_001739705.1:n.3607-295G=
XR_923313.2:n.4043-295G=
NM_000312.4:c.999C= MANE Select	NP_000303.1:p.Ala333=
NM_001375602.1:c.1182C=	NP_001362531.1:p.Ala394=
NM_001375603.1:c.1164C=	NP_001362532.1:p.Ala388=
NM_001375604.1:c.1062C=	NP_001362533.1:p.Ala354=
NM_001375605.1:c.1101C=	NP_001362534.1:p.Ala367=
NM_001375606.1:c.1167C=	NP_001362535.1:p.Ala389=
NM_001375607.1:c.1185C=	NP_001362536.1:p.Ala395=
NM_001375608.1:c.942C=	NP_001362537.1:p.Ala314=
NM_001375609.1:c.975C=	NP_001362538.1:p.Ala325=
NM_001375610.1:c.993C=	NP_001362539.1:p.Ala331=
NM_001375611.1:c.999C=	NP_001362540.1:p.Ala333=
NM_001375613.1:c.999C=	NP_001362542.1:p.Ala333=