Canonical Allele Identifier: CA1286884484

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428462C= , CM000664.2:g.127428462C=	GRCh38
NC_000002.11:g.128186038C= , CM000664.1:g.128186038C=	GRCh37
NC_000002.10:g.127902508C=	NCBI36
NG_016323.1:g.15043C= , LRG_599:g.15043C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000312.4:c.902C= MANE Select	NP_000303.1:p.Ala301=
ENST00000234071.8:c.902C= MANE Select	ENSP00000234071.4:p.Ala301=
NM_000312.3:c.902C= , LRG_599t1:c.902C=	NP_000303.1:p.Ala301=
NM_001375602.1:c.1085C=	NP_001362531.1:p.Ala362=
NM_001375603.1:c.1067C=	NP_001362532.1:p.Ala356=
NM_001375604.1:c.965C=	NP_001362533.1:p.Ala322=
NM_001375605.1:c.1004C=	NP_001362534.1:p.Ala335=
NM_001375606.1:c.1070C=	NP_001362535.1:p.Ala357=
NM_001375607.1:c.1088C=	NP_001362536.1:p.Ala363=
NM_001375608.1:c.845C=	NP_001362537.1:p.Ala282=
NM_001375609.1:c.878C=	NP_001362538.1:p.Ala293=
NM_001375610.1:c.896C=	NP_001362539.1:p.Ala299=
NM_001375611.1:c.902C=	NP_001362540.1:p.Ala301=
NM_001375613.1:c.902C=	NP_001362542.1:p.Ala301=
ENST00000234071.7:c.902C=	ENSP00000234071.3:p.Ala301=
ENST00000402125.2:c.226C=
ENST00000409048.1:c.1004C=	ENSP00000386679.1:p.Ala335=
XM_005263715.3:c.1085C=	XP_005263772.1:p.Ala362=
XM_005263716.3:c.1067C=	XP_005263773.1:p.Ala356=
XM_005263717.3:c.965C=	XP_005263774.1:p.Ala322=
XM_005263717.4:c.965C=	XP_005263774.1:p.Ala322=
XM_017004505.1:c.1145C=	XP_016859994.1:p.Ala382=
XM_024453002.1:c.1247C=	XP_024308770.1:p.Ala416=
XM_024453003.1:c.1187C=	XP_024308771.1:p.Ala396=
XM_024453004.1:c.1085C=	XP_024308772.1:p.Ala362=
XM_024453005.1:c.1067C=	XP_024308773.1:p.Ala356=
XM_024453006.1:c.1004C=	XP_024308774.1:p.Ala335=
XR_001739705.1:n.3607-198G=
XR_923313.1:n.1332-198G=
XR_923313.2:n.4043-198G=