Canonical Allele Identifier: CA1286884460

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428424C= , CM000664.2:g.127428424C=	GRCh38
NC_000002.11:g.128186000C= , CM000664.1:g.128186000C=	GRCh37
NC_000002.10:g.127902470C=	NCBI36
NG_016323.1:g.15005C= , LRG_599:g.15005C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.864C= MANE Select	ENSP00000234071.4:p.His288=
ENST00000234071.7:c.864C=	ENSP00000234071.3:p.His288=
ENST00000402125.2:c.188C=
ENST00000409048.1:c.966C=	ENSP00000386679.1:p.His322=
NM_000312.3:c.864C= , LRG_599t1:c.864C=	NP_000303.1:p.His288=
XM_005263715.3:c.1047C=	XP_005263772.1:p.His349=
XM_005263716.3:c.1029C=	XP_005263773.1:p.His343=
XM_005263717.3:c.927C=	XP_005263774.1:p.His309=
XR_923313.1:n.1332-160G=
XM_005263717.4:c.927C=	XP_005263774.1:p.His309=
XM_017004505.1:c.1107C=	XP_016859994.1:p.His369=
XM_024453002.1:c.1209C=	XP_024308770.1:p.His403=
XM_024453003.1:c.1149C=	XP_024308771.1:p.His383=
XM_024453004.1:c.1047C=	XP_024308772.1:p.His349=
XM_024453005.1:c.1029C=	XP_024308773.1:p.His343=
XM_024453006.1:c.966C=	XP_024308774.1:p.His322=
XR_001739705.1:n.3607-160G=
XR_923313.2:n.4043-160G=
NM_000312.4:c.864C= MANE Select	NP_000303.1:p.His288=
NM_001375602.1:c.1047C=	NP_001362531.1:p.His349=
NM_001375603.1:c.1029C=	NP_001362532.1:p.His343=
NM_001375604.1:c.927C=	NP_001362533.1:p.His309=
NM_001375605.1:c.966C=	NP_001362534.1:p.His322=
NM_001375606.1:c.1032C=	NP_001362535.1:p.His344=
NM_001375607.1:c.1050C=	NP_001362536.1:p.His350=
NM_001375608.1:c.807C=	NP_001362537.1:p.His269=
NM_001375609.1:c.840C=	NP_001362538.1:p.His280=
NM_001375610.1:c.858C=	NP_001362539.1:p.His286=
NM_001375611.1:c.864C=	NP_001362540.1:p.His288=
NM_001375613.1:c.864C=	NP_001362542.1:p.His288=