Canonical Allele Identifier: CA1286884527

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428560G= , CM000664.2:g.127428560G=	GRCh38
NC_000002.11:g.128186136G= , CM000664.1:g.128186136G=	GRCh37
NC_000002.10:g.127902606G=	NCBI36
NG_016323.1:g.15141G= , LRG_599:g.15141G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.1000G= MANE Select	ENSP00000234071.4:p.Gly334=
ENST00000234071.7:c.1000G=	ENSP00000234071.3:p.Gly334=
ENST00000402125.2:c.324G=
ENST00000409048.1:c.1102G=	ENSP00000386679.1:p.Gly368=
NM_000312.3:c.1000G= , LRG_599t1:c.1000G=	NP_000303.1:p.Gly334=
XM_005263715.3:c.1183G=	XP_005263772.1:p.Gly395=
XM_005263716.3:c.1165G=	XP_005263773.1:p.Gly389=
XM_005263717.3:c.1063G=	XP_005263774.1:p.Gly355=
XR_923313.1:n.1332-296C=
XM_005263717.4:c.1063G=	XP_005263774.1:p.Gly355=
XM_017004505.1:c.1243G=	XP_016859994.1:p.Gly415=
XM_024453002.1:c.1345G=	XP_024308770.1:p.Gly449=
XM_024453003.1:c.1285G=	XP_024308771.1:p.Gly429=
XM_024453004.1:c.1183G=	XP_024308772.1:p.Gly395=
XM_024453005.1:c.1165G=	XP_024308773.1:p.Gly389=
XM_024453006.1:c.1102G=	XP_024308774.1:p.Gly368=
XR_001739705.1:n.3607-296C=
XR_923313.2:n.4043-296C=
NM_000312.4:c.1000G= MANE Select	NP_000303.1:p.Gly334=
NM_001375602.1:c.1183G=	NP_001362531.1:p.Gly395=
NM_001375603.1:c.1165G=	NP_001362532.1:p.Gly389=
NM_001375604.1:c.1063G=	NP_001362533.1:p.Gly355=
NM_001375605.1:c.1102G=	NP_001362534.1:p.Gly368=
NM_001375606.1:c.1168G=	NP_001362535.1:p.Gly390=
NM_001375607.1:c.1186G=	NP_001362536.1:p.Gly396=
NM_001375608.1:c.943G=	NP_001362537.1:p.Gly315=
NM_001375609.1:c.976G=	NP_001362538.1:p.Gly326=
NM_001375610.1:c.994G=	NP_001362539.1:p.Gly332=
NM_001375611.1:c.1000G=	NP_001362540.1:p.Gly334=
NM_001375613.1:c.1000G=	NP_001362542.1:p.Gly334=