Canonical Allele Identifier: CA1286884553

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428614G= , CM000664.2:g.127428614G=	GRCh38
NC_000002.11:g.128186190G= , CM000664.1:g.128186190G=	GRCh37
NC_000002.10:g.127902660G=	NCBI36
NG_016323.1:g.15195G= , LRG_599:g.15195G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.1054G= MANE Select	ENSP00000234071.4:p.Ala352=
ENST00000234071.7:c.1054G=	ENSP00000234071.3:p.Ala352=
ENST00000402125.2:c.378G=
ENST00000409048.1:c.1156G=	ENSP00000386679.1:p.Ala386=
NM_000312.3:c.1054G= , LRG_599t1:c.1054G=	NP_000303.1:p.Ala352=
XM_005263715.3:c.1237G=	XP_005263772.1:p.Ala413=
XM_005263716.3:c.1219G=	XP_005263773.1:p.Ala407=
XM_005263717.3:c.1117G=	XP_005263774.1:p.Ala373=
XR_923313.1:n.1332-350C=
XM_005263717.4:c.1117G=	XP_005263774.1:p.Ala373=
XM_017004505.1:c.1297G=	XP_016859994.1:p.Ala433=
XM_024453002.1:c.1399G=	XP_024308770.1:p.Ala467=
XM_024453003.1:c.1339G=	XP_024308771.1:p.Ala447=
XM_024453004.1:c.1237G=	XP_024308772.1:p.Ala413=
XM_024453005.1:c.1219G=	XP_024308773.1:p.Ala407=
XM_024453006.1:c.1156G=	XP_024308774.1:p.Ala386=
XR_001739705.1:n.3607-350C=
XR_923313.2:n.4043-350C=
NM_000312.4:c.1054G= MANE Select	NP_000303.1:p.Ala352=
NM_001375602.1:c.1237G=	NP_001362531.1:p.Ala413=
NM_001375603.1:c.1219G=	NP_001362532.1:p.Ala407=
NM_001375604.1:c.1117G=	NP_001362533.1:p.Ala373=
NM_001375605.1:c.1156G=	NP_001362534.1:p.Ala386=
NM_001375606.1:c.1222G=	NP_001362535.1:p.Ala408=
NM_001375607.1:c.1240G=	NP_001362536.1:p.Ala414=
NM_001375608.1:c.997G=	NP_001362537.1:p.Ala333=
NM_001375609.1:c.1030G=	NP_001362538.1:p.Ala344=
NM_001375610.1:c.1048G=	NP_001362539.1:p.Ala350=
NM_001375611.1:c.1054G=	NP_001362540.1:p.Ala352=
NM_001375613.1:c.1054G=	NP_001362542.1:p.Ala352=