Canonical Allele Identifier: CA1286884437

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428375G= , CM000664.2:g.127428375G=	GRCh38
NC_000002.11:g.128185951G= , CM000664.1:g.128185951G=	GRCh37
NC_000002.10:g.127902421G=	NCBI36
NG_016323.1:g.14956G= , LRG_599:g.14956G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.815G= MANE Select	ENSP00000234071.4:p.Arg272=
ENST00000234071.7:c.815G=	ENSP00000234071.3:p.Arg272=
ENST00000402125.2:c.139G=
ENST00000409048.1:c.917G=	ENSP00000386679.1:p.Arg306=
NM_000312.3:c.815G= , LRG_599t1:c.815G=	NP_000303.1:p.Arg272=
XM_005263715.3:c.998G=	XP_005263772.1:p.Arg333=
XM_005263716.3:c.980G=	XP_005263773.1:p.Arg327=
XM_005263717.3:c.878G=	XP_005263774.1:p.Arg293=
XR_923313.1:n.1332-111C=
XM_005263717.4:c.878G=	XP_005263774.1:p.Arg293=
XM_017004505.1:c.1058G=	XP_016859994.1:p.Arg353=
XM_024453002.1:c.1160G=	XP_024308770.1:p.Arg387=
XM_024453003.1:c.1100G=	XP_024308771.1:p.Arg367=
XM_024453004.1:c.998G=	XP_024308772.1:p.Arg333=
XM_024453005.1:c.980G=	XP_024308773.1:p.Arg327=
XM_024453006.1:c.917G=	XP_024308774.1:p.Arg306=
XR_001739705.1:n.3607-111C=
XR_923313.2:n.4043-111C=
NM_000312.4:c.815G= MANE Select	NP_000303.1:p.Arg272=
NM_001375602.1:c.998G=	NP_001362531.1:p.Arg333=
NM_001375603.1:c.980G=	NP_001362532.1:p.Arg327=
NM_001375604.1:c.878G=	NP_001362533.1:p.Arg293=
NM_001375605.1:c.917G=	NP_001362534.1:p.Arg306=
NM_001375606.1:c.983G=	NP_001362535.1:p.Arg328=
NM_001375607.1:c.1001G=	NP_001362536.1:p.Arg334=
NM_001375608.1:c.758G=	NP_001362537.1:p.Arg253=
NM_001375609.1:c.791G=	NP_001362538.1:p.Arg264=
NM_001375610.1:c.809G=	NP_001362539.1:p.Arg270=
NM_001375611.1:c.815G=	NP_001362540.1:p.Arg272=
NM_001375613.1:c.815G=	NP_001362542.1:p.Arg272=