Canonical Allele Identifier: CA1286884638

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428767G= , CM000664.2:g.127428767G=	GRCh38
NC_000002.11:g.128186343G= , CM000664.1:g.128186343G=	GRCh37
NC_000002.10:g.127902813G=	NCBI36
NG_016323.1:g.15348G= , LRG_599:g.15348G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.1207G= MANE Select	ENSP00000234071.4:p.Gly403=
ENST00000234071.7:c.1207G=	ENSP00000234071.3:p.Gly403=
ENST00000402125.2:c.531G=
ENST00000409048.1:c.1309G=	ENSP00000386679.1:p.Gly437=
NM_000312.3:c.1207G= , LRG_599t1:c.1207G=	NP_000303.1:p.Gly403=
XM_005263715.3:c.1390G=	XP_005263772.1:p.Gly464=
XM_005263716.3:c.1372G=	XP_005263773.1:p.Gly458=
XM_005263717.3:c.1270G=	XP_005263774.1:p.Gly424=
XR_923313.1:n.1332-503C=
XM_005263717.4:c.1270G=	XP_005263774.1:p.Gly424=
XM_017004505.1:c.1450G=	XP_016859994.1:p.Gly484=
XM_024453002.1:c.1552G=	XP_024308770.1:p.Gly518=
XM_024453003.1:c.1492G=	XP_024308771.1:p.Gly498=
XM_024453004.1:c.1390G=	XP_024308772.1:p.Gly464=
XM_024453005.1:c.1372G=	XP_024308773.1:p.Gly458=
XM_024453006.1:c.1309G=	XP_024308774.1:p.Gly437=
XR_001739705.1:n.3607-503C=
XR_923313.2:n.4043-503C=
NM_000312.4:c.1207G= MANE Select	NP_000303.1:p.Gly403=
NM_001375602.1:c.1390G=	NP_001362531.1:p.Gly464=
NM_001375603.1:c.1372G=	NP_001362532.1:p.Gly458=
NM_001375604.1:c.1270G=	NP_001362533.1:p.Gly424=
NM_001375605.1:c.1309G=	NP_001362534.1:p.Gly437=
NM_001375606.1:c.1375G=	NP_001362535.1:p.Gly459=
NM_001375607.1:c.1393G=	NP_001362536.1:p.Gly465=
NM_001375608.1:c.1150G=	NP_001362537.1:p.Gly384=
NM_001375609.1:c.1183G=	NP_001362538.1:p.Gly395=
NM_001375610.1:c.1201G=	NP_001362539.1:p.Gly401=
NM_001375611.1:c.1207G=	NP_001362540.1:p.Gly403=
NM_001375613.1:c.1207G=	NP_001362542.1:p.Gly403=