Canonical Allele Identifier: CA428872875

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128186405T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428829T>C , CM000664.2:g.127428829T>C	GRCh38
NC_000002.11:g.128186405T>C , CM000664.1:g.128186405T>C	GRCh37
NC_000002.10:g.127902875T>C	NCBI36
NG_016323.1:g.15410T>C , LRG_599:g.15410T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000234071.8:c.1269T>C MANE Select	ENSP00000234071.4:p.Gly423=
ENST00000234071.7:c.1269T>C	ENSP00000234071.3:p.Gly423=
ENST00000402125.2:c.593T>C
ENST00000409048.1:c.1371T>C	ENSP00000386679.1:p.Gly457=
NM_000312.3:c.1269T>C , LRG_599t1:c.1269T>C	NP_000303.1:p.Gly423=
XM_005263715.3:c.1452T>C	XP_005263772.1:p.Gly484=
XM_005263716.3:c.1434T>C	XP_005263773.1:p.Gly478=
XM_005263717.3:c.1332T>C	XP_005263774.1:p.Gly444=
XR_923313.1:n.1332-565A>G
XM_005263717.4:c.1332T>C	XP_005263774.1:p.Gly444=
XM_017004505.1:c.1512T>C	XP_016859994.1:p.Gly504=
XM_024453002.1:c.1614T>C	XP_024308770.1:p.Gly538=
XM_024453003.1:c.1554T>C	XP_024308771.1:p.Gly518=
XM_024453004.1:c.1452T>C	XP_024308772.1:p.Gly484=
XM_024453005.1:c.1434T>C	XP_024308773.1:p.Gly478=
XM_024453006.1:c.1371T>C	XP_024308774.1:p.Gly457=
XR_001739705.1:n.3607-565A>G
XR_923313.2:n.4043-565A>G
NM_000312.4:c.1269T>C MANE Select	NP_000303.1:p.Gly423=
NM_001375602.1:c.1452T>C	NP_001362531.1:p.Gly484=
NM_001375603.1:c.1434T>C	NP_001362532.1:p.Gly478=
NM_001375604.1:c.1332T>C	NP_001362533.1:p.Gly444=
NM_001375605.1:c.1371T>C	NP_001362534.1:p.Gly457=
NM_001375606.1:c.1437T>C	NP_001362535.1:p.Gly479=
NM_001375607.1:c.1455T>C	NP_001362536.1:p.Gly485=
NM_001375608.1:c.1212T>C	NP_001362537.1:p.Gly404=
NM_001375609.1:c.1245T>C	NP_001362538.1:p.Gly415=
NM_001375610.1:c.1263T>C	NP_001362539.1:p.Gly421=
NM_001375611.1:c.1269T>C	NP_001362540.1:p.Gly423=
NM_001375613.1:c.1269T>C	NP_001362542.1:p.Gly423=