Canonical Allele Identifier: CA1286883399

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127426096T= , CM000664.2:g.127426096T=	GRCh38
NC_000002.11:g.128183672T= , CM000664.1:g.128183672T=	GRCh37
NC_000002.10:g.127900142T=	NCBI36
NG_016323.1:g.12677T= , LRG_599:g.12677T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.547T= MANE Select	ENSP00000234071.4:p.Cys183=
ENST00000234071.7:c.547T=	ENSP00000234071.3:p.Cys183=
ENST00000402125.2:c.121-2261T=
ENST00000409048.1:c.649T=	ENSP00000386679.1:p.Cys217=
ENST00000442644.5:c.490T=	ENSP00000411241.1:p.Cys164=
ENST00000464089.1:n.133T=
NM_000312.3:c.547T= , LRG_599t1:c.547T=	NP_000303.1:p.Cys183=
XM_005263715.3:c.730T=	XP_005263772.1:p.Cys244=
XM_005263716.3:c.712T=	XP_005263773.1:p.Cys238=
XM_005263717.3:c.610T=	XP_005263774.1:p.Cys204=
XM_005263717.4:c.610T=	XP_005263774.1:p.Cys204=
XM_017004505.1:c.790T=	XP_016859994.1:p.Cys264=
XM_024453002.1:c.892T=	XP_024308770.1:p.Cys298=
XM_024453003.1:c.832T=	XP_024308771.1:p.Cys278=
XM_024453004.1:c.730T=	XP_024308772.1:p.Cys244=
XM_024453005.1:c.712T=	XP_024308773.1:p.Cys238=
XM_024453006.1:c.649T=	XP_024308774.1:p.Cys217=
XR_923313.2:n.4489A=
NM_000312.4:c.547T= MANE Select	NP_000303.1:p.Cys183=
NM_001375602.1:c.730T=	NP_001362531.1:p.Cys244=
NM_001375603.1:c.712T=	NP_001362532.1:p.Cys238=
NM_001375604.1:c.610T=	NP_001362533.1:p.Cys204=
NM_001375605.1:c.649T=	NP_001362534.1:p.Cys217=
NM_001375606.1:c.715T=	NP_001362535.1:p.Cys239=
NM_001375607.1:c.733T=	NP_001362536.1:p.Cys245=
NM_001375608.1:c.490T=	NP_001362537.1:p.Cys164=
NM_001375609.1:c.523T=	NP_001362538.1:p.Cys175=
NM_001375610.1:c.541T=	NP_001362539.1:p.Cys181=
NM_001375611.1:c.547T=	NP_001362540.1:p.Cys183=
NM_001375613.1:c.547T=	NP_001362542.1:p.Cys183=