Canonical Allele Identifier: CA1286884604

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428721T= , CM000664.2:g.127428721T=	GRCh38
NC_000002.11:g.128186297T= , CM000664.1:g.128186297T=	GRCh37
NC_000002.10:g.127902767T=	NCBI36
NG_016323.1:g.15302T= , LRG_599:g.15302T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000234071.8:c.1161T= MANE Select	ENSP00000234071.4:p.Cys387=
ENST00000234071.7:c.1161T=	ENSP00000234071.3:p.Cys387=
ENST00000402125.2:c.485T=
ENST00000409048.1:c.1263T=	ENSP00000386679.1:p.Cys421=
NM_000312.3:c.1161T= , LRG_599t1:c.1161T=	NP_000303.1:p.Cys387=
XM_005263715.3:c.1344T=	XP_005263772.1:p.Cys448=
XM_005263716.3:c.1326T=	XP_005263773.1:p.Cys442=
XM_005263717.3:c.1224T=	XP_005263774.1:p.Cys408=
XR_923313.1:n.1332-457A=
XM_005263717.4:c.1224T=	XP_005263774.1:p.Cys408=
XM_017004505.1:c.1404T=	XP_016859994.1:p.Cys468=
XM_024453002.1:c.1506T=	XP_024308770.1:p.Cys502=
XM_024453003.1:c.1446T=	XP_024308771.1:p.Cys482=
XM_024453004.1:c.1344T=	XP_024308772.1:p.Cys448=
XM_024453005.1:c.1326T=	XP_024308773.1:p.Cys442=
XM_024453006.1:c.1263T=	XP_024308774.1:p.Cys421=
XR_001739705.1:n.3607-457A=
XR_923313.2:n.4043-457A=
NM_000312.4:c.1161T= MANE Select	NP_000303.1:p.Cys387=
NM_001375602.1:c.1344T=	NP_001362531.1:p.Cys448=
NM_001375603.1:c.1326T=	NP_001362532.1:p.Cys442=
NM_001375604.1:c.1224T=	NP_001362533.1:p.Cys408=
NM_001375605.1:c.1263T=	NP_001362534.1:p.Cys421=
NM_001375606.1:c.1329T=	NP_001362535.1:p.Cys443=
NM_001375607.1:c.1347T=	NP_001362536.1:p.Cys449=
NM_001375608.1:c.1104T=	NP_001362537.1:p.Cys368=
NM_001375609.1:c.1137T=	NP_001362538.1:p.Cys379=
NM_001375610.1:c.1155T=	NP_001362539.1:p.Cys385=
NM_001375611.1:c.1161T=	NP_001362540.1:p.Cys387=
NM_001375613.1:c.1161T=	NP_001362542.1:p.Cys387=