Canonical Allele Identifier: CA1286884621

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428741G= , CM000664.2:g.127428741G=	GRCh38
NC_000002.11:g.128186317G= , CM000664.1:g.128186317G=	GRCh37
NC_000002.10:g.127902787G=	NCBI36
NG_016323.1:g.15322G= , LRG_599:g.15322G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000234071.8:c.1181G= MANE Select	ENSP00000234071.4:p.Arg394=
ENST00000234071.7:c.1181G=	ENSP00000234071.3:p.Arg394=
ENST00000402125.2:c.505G=
ENST00000409048.1:c.1283G=	ENSP00000386679.1:p.Arg428=
NM_000312.3:c.1181G= , LRG_599t1:c.1181G=	NP_000303.1:p.Arg394=
XM_005263715.3:c.1364G=	XP_005263772.1:p.Arg455=
XM_005263716.3:c.1346G=	XP_005263773.1:p.Arg449=
XM_005263717.3:c.1244G=	XP_005263774.1:p.Arg415=
XR_923313.1:n.1332-477C=
XM_005263717.4:c.1244G=	XP_005263774.1:p.Arg415=
XM_017004505.1:c.1424G=	XP_016859994.1:p.Arg475=
XM_024453002.1:c.1526G=	XP_024308770.1:p.Arg509=
XM_024453003.1:c.1466G=	XP_024308771.1:p.Arg489=
XM_024453004.1:c.1364G=	XP_024308772.1:p.Arg455=
XM_024453005.1:c.1346G=	XP_024308773.1:p.Arg449=
XM_024453006.1:c.1283G=	XP_024308774.1:p.Arg428=
XR_001739705.1:n.3607-477C=
XR_923313.2:n.4043-477C=
NM_000312.4:c.1181G= MANE Select	NP_000303.1:p.Arg394=
NM_001375602.1:c.1364G=	NP_001362531.1:p.Arg455=
NM_001375603.1:c.1346G=	NP_001362532.1:p.Arg449=
NM_001375604.1:c.1244G=	NP_001362533.1:p.Arg415=
NM_001375605.1:c.1283G=	NP_001362534.1:p.Arg428=
NM_001375606.1:c.1349G=	NP_001362535.1:p.Arg450=
NM_001375607.1:c.1367G=	NP_001362536.1:p.Arg456=
NM_001375608.1:c.1124G=	NP_001362537.1:p.Arg375=
NM_001375609.1:c.1157G=	NP_001362538.1:p.Arg386=
NM_001375610.1:c.1175G=	NP_001362539.1:p.Arg392=
NM_001375611.1:c.1181G=	NP_001362540.1:p.Arg394=
NM_001375613.1:c.1181G=	NP_001362542.1:p.Arg394=