Canonical Allele Identifier: CA1286884431

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428367C= , CM000664.2:g.127428367C=	GRCh38
NC_000002.11:g.128185943C= , CM000664.1:g.128185943C=	GRCh37
NC_000002.10:g.127902413C=	NCBI36
NG_016323.1:g.14948C= , LRG_599:g.14948C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000234071.8:c.807C= MANE Select	ENSP00000234071.4:p.Asp269=
ENST00000234071.7:c.807C=	ENSP00000234071.3:p.Asp269=
ENST00000402125.2:c.131C=
ENST00000409048.1:c.909C=	ENSP00000386679.1:p.Asp303=
NM_000312.3:c.807C= , LRG_599t1:c.807C=	NP_000303.1:p.Asp269=
XM_005263715.3:c.990C=	XP_005263772.1:p.Asp330=
XM_005263716.3:c.972C=	XP_005263773.1:p.Asp324=
XM_005263717.3:c.870C=	XP_005263774.1:p.Asp290=
XR_923313.1:n.1332-103G=
XM_005263717.4:c.870C=	XP_005263774.1:p.Asp290=
XM_017004505.1:c.1050C=	XP_016859994.1:p.Asp350=
XM_024453002.1:c.1152C=	XP_024308770.1:p.Asp384=
XM_024453003.1:c.1092C=	XP_024308771.1:p.Asp364=
XM_024453004.1:c.990C=	XP_024308772.1:p.Asp330=
XM_024453005.1:c.972C=	XP_024308773.1:p.Asp324=
XM_024453006.1:c.909C=	XP_024308774.1:p.Asp303=
XR_001739705.1:n.3607-103G=
XR_923313.2:n.4043-103G=
NM_000312.4:c.807C= MANE Select	NP_000303.1:p.Asp269=
NM_001375602.1:c.990C=	NP_001362531.1:p.Asp330=
NM_001375603.1:c.972C=	NP_001362532.1:p.Asp324=
NM_001375604.1:c.870C=	NP_001362533.1:p.Asp290=
NM_001375605.1:c.909C=	NP_001362534.1:p.Asp303=
NM_001375606.1:c.975C=	NP_001362535.1:p.Asp325=
NM_001375607.1:c.993C=	NP_001362536.1:p.Asp331=
NM_001375608.1:c.750C=	NP_001362537.1:p.Asp250=
NM_001375609.1:c.783C=	NP_001362538.1:p.Asp261=
NM_001375610.1:c.801C=	NP_001362539.1:p.Asp267=
NM_001375611.1:c.807C=	NP_001362540.1:p.Asp269=
NM_001375613.1:c.807C=	NP_001362542.1:p.Asp269=