Canonical Allele Identifier: CA1286883400

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127426097G= , CM000664.2:g.127426097G=	GRCh38
NC_000002.11:g.128183673G= , CM000664.1:g.128183673G=	GRCh37
NC_000002.10:g.127900143G=	NCBI36
NG_016323.1:g.12678G= , LRG_599:g.12678G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.548G= MANE Select	ENSP00000234071.4:p.Cys183=
ENST00000234071.7:c.548G=	ENSP00000234071.3:p.Cys183=
ENST00000402125.2:c.121-2260G=
ENST00000409048.1:c.650G=	ENSP00000386679.1:p.Cys217=
ENST00000442644.5:c.491G=	ENSP00000411241.1:p.Cys164=
ENST00000464089.1:n.134G=
NM_000312.3:c.548G= , LRG_599t1:c.548G=	NP_000303.1:p.Cys183=
XM_005263715.3:c.731G=	XP_005263772.1:p.Cys244=
XM_005263716.3:c.713G=	XP_005263773.1:p.Cys238=
XM_005263717.3:c.611G=	XP_005263774.1:p.Cys204=
XM_005263717.4:c.611G=	XP_005263774.1:p.Cys204=
XM_017004505.1:c.791G=	XP_016859994.1:p.Cys264=
XM_024453002.1:c.893G=	XP_024308770.1:p.Cys298=
XM_024453003.1:c.833G=	XP_024308771.1:p.Cys278=
XM_024453004.1:c.731G=	XP_024308772.1:p.Cys244=
XM_024453005.1:c.713G=	XP_024308773.1:p.Cys238=
XM_024453006.1:c.650G=	XP_024308774.1:p.Cys217=
XR_923313.2:n.4488C=
NM_000312.4:c.548G= MANE Select	NP_000303.1:p.Cys183=
NM_001375602.1:c.731G=	NP_001362531.1:p.Cys244=
NM_001375603.1:c.713G=	NP_001362532.1:p.Cys238=
NM_001375604.1:c.611G=	NP_001362533.1:p.Cys204=
NM_001375605.1:c.650G=	NP_001362534.1:p.Cys217=
NM_001375606.1:c.716G=	NP_001362535.1:p.Cys239=
NM_001375607.1:c.734G=	NP_001362536.1:p.Cys245=
NM_001375608.1:c.491G=	NP_001362537.1:p.Cys164=
NM_001375609.1:c.524G=	NP_001362538.1:p.Cys175=
NM_001375610.1:c.542G=	NP_001362539.1:p.Cys181=
NM_001375611.1:c.548G=	NP_001362540.1:p.Cys183=
NM_001375613.1:c.548G=	NP_001362542.1:p.Cys183=