Canonical Allele Identifier: CA1286884649

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428783C= , CM000664.2:g.127428783C=	GRCh38
NC_000002.11:g.128186359C= , CM000664.1:g.128186359C=	GRCh37
NC_000002.10:g.127902829C=	NCBI36
NG_016323.1:g.15364C= , LRG_599:g.15364C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.1223C= MANE Select	ENSP00000234071.4:p.Ala408=
ENST00000234071.7:c.1223C=	ENSP00000234071.3:p.Ala408=
ENST00000402125.2:c.547C=
ENST00000409048.1:c.1325C=	ENSP00000386679.1:p.Ala442=
NM_000312.3:c.1223C= , LRG_599t1:c.1223C=	NP_000303.1:p.Ala408=
XM_005263715.3:c.1406C=	XP_005263772.1:p.Ala469=
XM_005263716.3:c.1388C=	XP_005263773.1:p.Ala463=
XM_005263717.3:c.1286C=	XP_005263774.1:p.Ala429=
XR_923313.1:n.1332-519G=
XM_005263717.4:c.1286C=	XP_005263774.1:p.Ala429=
XM_017004505.1:c.1466C=	XP_016859994.1:p.Ala489=
XM_024453002.1:c.1568C=	XP_024308770.1:p.Ala523=
XM_024453003.1:c.1508C=	XP_024308771.1:p.Ala503=
XM_024453004.1:c.1406C=	XP_024308772.1:p.Ala469=
XM_024453005.1:c.1388C=	XP_024308773.1:p.Ala463=
XM_024453006.1:c.1325C=	XP_024308774.1:p.Ala442=
XR_001739705.1:n.3607-519G=
XR_923313.2:n.4043-519G=
NM_000312.4:c.1223C= MANE Select	NP_000303.1:p.Ala408=
NM_001375602.1:c.1406C=	NP_001362531.1:p.Ala469=
NM_001375603.1:c.1388C=	NP_001362532.1:p.Ala463=
NM_001375604.1:c.1286C=	NP_001362533.1:p.Ala429=
NM_001375605.1:c.1325C=	NP_001362534.1:p.Ala442=
NM_001375606.1:c.1391C=	NP_001362535.1:p.Ala464=
NM_001375607.1:c.1409C=	NP_001362536.1:p.Ala470=
NM_001375608.1:c.1166C=	NP_001362537.1:p.Ala389=
NM_001375609.1:c.1199C=	NP_001362538.1:p.Ala400=
NM_001375610.1:c.1217C=	NP_001362539.1:p.Ala406=
NM_001375611.1:c.1223C=	NP_001362540.1:p.Ala408=
NM_001375613.1:c.1223C=	NP_001362542.1:p.Ala408=