Canonical Allele Identifier: CA1286882168

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127423397G= , CM000664.2:g.127423397G=	GRCh38
NC_000002.11:g.128180973G= , CM000664.1:g.128180973G=	GRCh37
NC_000002.10:g.127897443G=	NCBI36
NG_016323.1:g.9978G= , LRG_599:g.9978G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.524G= MANE Select	ENSP00000234071.4:p.Cys175=
ENST00000234071.7:c.524G=	ENSP00000234071.3:p.Cys175=
ENST00000402125.2:c.109G=
ENST00000409048.1:c.626G=	ENSP00000386679.1:p.Cys209=
ENST00000442644.5:c.467G=	ENSP00000411241.1:p.Cys156=
ENST00000464089.1:n.110G=
NM_000312.3:c.524G= , LRG_599t1:c.524G=	NP_000303.1:p.Cys175=
XM_005263715.3:c.707G=	XP_005263772.1:p.Cys236=
XM_005263716.3:c.689G=	XP_005263773.1:p.Cys230=
XM_005263717.3:c.587G=	XP_005263774.1:p.Cys196=
XM_005263717.4:c.587G=	XP_005263774.1:p.Cys196=
XM_017004505.1:c.767G=	XP_016859994.1:p.Cys256=
XM_024453002.1:c.869G=	XP_024308770.1:p.Cys290=
XM_024453003.1:c.809G=	XP_024308771.1:p.Cys270=
XM_024453004.1:c.707G=	XP_024308772.1:p.Cys236=
XM_024453005.1:c.689G=	XP_024308773.1:p.Cys230=
XM_024453006.1:c.626G=	XP_024308774.1:p.Cys209=
NM_000312.4:c.524G= MANE Select	NP_000303.1:p.Cys175=
NM_001375602.1:c.707G=	NP_001362531.1:p.Cys236=
NM_001375603.1:c.689G=	NP_001362532.1:p.Cys230=
NM_001375604.1:c.587G=	NP_001362533.1:p.Cys196=
NM_001375605.1:c.626G=	NP_001362534.1:p.Cys209=
NM_001375606.1:c.692G=	NP_001362535.1:p.Cys231=
NM_001375607.1:c.710G=	NP_001362536.1:p.Cys237=
NM_001375608.1:c.467G=	NP_001362537.1:p.Cys156=
NM_001375609.1:c.500G=	NP_001362538.1:p.Cys167=
NM_001375610.1:c.518G=	NP_001362539.1:p.Cys173=
NM_001375611.1:c.524G=	NP_001362540.1:p.Cys175=
NM_001375613.1:c.524G=	NP_001362542.1:p.Cys175=