Canonical Allele Identifier: CA428872174

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128186316C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428740C>A , CM000664.2:g.127428740C>A	GRCh38
NC_000002.11:g.128186316C>A , CM000664.1:g.128186316C>A	GRCh37
NC_000002.10:g.127902786C>A	NCBI36
NG_016323.1:g.15321C>A , LRG_599:g.15321C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000234071.8:c.1180C>A MANE Select	ENSP00000234071.4:p.Arg394=
ENST00000234071.7:c.1180C>A	ENSP00000234071.3:p.Arg394=
ENST00000402125.2:c.504C>A
ENST00000409048.1:c.1282C>A	ENSP00000386679.1:p.Arg428=
NM_000312.3:c.1180C>A , LRG_599t1:c.1180C>A	NP_000303.1:p.Arg394=
XM_005263715.3:c.1363C>A	XP_005263772.1:p.Arg455=
XM_005263716.3:c.1345C>A	XP_005263773.1:p.Arg449=
XM_005263717.3:c.1243C>A	XP_005263774.1:p.Arg415=
XR_923313.1:n.1332-476G>T
XM_005263717.4:c.1243C>A	XP_005263774.1:p.Arg415=
XM_017004505.1:c.1423C>A	XP_016859994.1:p.Arg475=
XM_024453002.1:c.1525C>A	XP_024308770.1:p.Arg509=
XM_024453003.1:c.1465C>A	XP_024308771.1:p.Arg489=
XM_024453004.1:c.1363C>A	XP_024308772.1:p.Arg455=
XM_024453005.1:c.1345C>A	XP_024308773.1:p.Arg449=
XM_024453006.1:c.1282C>A	XP_024308774.1:p.Arg428=
XR_001739705.1:n.3607-476G>T
XR_923313.2:n.4043-476G>T
NM_000312.4:c.1180C>A MANE Select	NP_000303.1:p.Arg394=
NM_001375602.1:c.1363C>A	NP_001362531.1:p.Arg455=
NM_001375603.1:c.1345C>A	NP_001362532.1:p.Arg449=
NM_001375604.1:c.1243C>A	NP_001362533.1:p.Arg415=
NM_001375605.1:c.1282C>A	NP_001362534.1:p.Arg428=
NM_001375606.1:c.1348C>A	NP_001362535.1:p.Arg450=
NM_001375607.1:c.1366C>A	NP_001362536.1:p.Arg456=
NM_001375608.1:c.1123C>A	NP_001362537.1:p.Arg375=
NM_001375609.1:c.1156C>A	NP_001362538.1:p.Arg386=
NM_001375610.1:c.1174C>A	NP_001362539.1:p.Arg392=
NM_001375611.1:c.1180C>A	NP_001362540.1:p.Arg394=
NM_001375613.1:c.1180C>A	NP_001362542.1:p.Arg394=