Canonical Allele Identifier: CA1286884497

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428487C= , CM000664.2:g.127428487C=	GRCh38
NC_000002.11:g.128186063C= , CM000664.1:g.128186063C=	GRCh37
NC_000002.10:g.127902533C=	NCBI36
NG_016323.1:g.15068C= , LRG_599:g.15068C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.927C= MANE Select	ENSP00000234071.4:p.Ala309=
ENST00000234071.7:c.927C=	ENSP00000234071.3:p.Ala309=
ENST00000402125.2:c.251C=
ENST00000409048.1:c.1029C=	ENSP00000386679.1:p.Ala343=
NM_000312.3:c.927C= , LRG_599t1:c.927C=	NP_000303.1:p.Ala309=
XM_005263715.3:c.1110C=	XP_005263772.1:p.Ala370=
XM_005263716.3:c.1092C=	XP_005263773.1:p.Ala364=
XM_005263717.3:c.990C=	XP_005263774.1:p.Ala330=
XR_923313.1:n.1332-223G=
XM_005263717.4:c.990C=	XP_005263774.1:p.Ala330=
XM_017004505.1:c.1170C=	XP_016859994.1:p.Ala390=
XM_024453002.1:c.1272C=	XP_024308770.1:p.Ala424=
XM_024453003.1:c.1212C=	XP_024308771.1:p.Ala404=
XM_024453004.1:c.1110C=	XP_024308772.1:p.Ala370=
XM_024453005.1:c.1092C=	XP_024308773.1:p.Ala364=
XM_024453006.1:c.1029C=	XP_024308774.1:p.Ala343=
XR_001739705.1:n.3607-223G=
XR_923313.2:n.4043-223G=
NM_000312.4:c.927C= MANE Select	NP_000303.1:p.Ala309=
NM_001375602.1:c.1110C=	NP_001362531.1:p.Ala370=
NM_001375603.1:c.1092C=	NP_001362532.1:p.Ala364=
NM_001375604.1:c.990C=	NP_001362533.1:p.Ala330=
NM_001375605.1:c.1029C=	NP_001362534.1:p.Ala343=
NM_001375606.1:c.1095C=	NP_001362535.1:p.Ala365=
NM_001375607.1:c.1113C=	NP_001362536.1:p.Ala371=
NM_001375608.1:c.870C=	NP_001362537.1:p.Ala290=
NM_001375609.1:c.903C=	NP_001362538.1:p.Ala301=
NM_001375610.1:c.921C=	NP_001362539.1:p.Ala307=
NM_001375611.1:c.927C=	NP_001362540.1:p.Ala309=
NM_001375613.1:c.927C=	NP_001362542.1:p.Ala309=