Canonical Allele Identifier: CA1286884672
Gene: PROC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127428831A= , CM000664.2:g.127428831A= GRCh38
NC_000002.11:g.128186407A= , CM000664.1:g.128186407A= GRCh37
NC_000002.10:g.127902877A= NCBI36
NG_016323.1:g.15412A= , LRG_599:g.15412A=

Transcript Alleles

HGVS Amino-acid change
ENST00000234071.8:c.1271A= MANE Select ENSP00000234071.4:p.Glu424=
ENST00000234071.7:c.1271A= ENSP00000234071.3:p.Glu424=
ENST00000402125.2:c.595A=
ENST00000409048.1:c.1373A= ENSP00000386679.1:p.Glu458=
NM_000312.3:c.1271A= , LRG_599t1:c.1271A= NP_000303.1:p.Glu424=
XM_005263715.3:c.1454A= XP_005263772.1:p.Glu485=
XM_005263716.3:c.1436A= XP_005263773.1:p.Glu479=
XM_005263717.3:c.1334A= XP_005263774.1:p.Glu445=
XR_923313.1:n.1332-567T=
XM_005263717.4:c.1334A= XP_005263774.1:p.Glu445=
XM_017004505.1:c.1514A= XP_016859994.1:p.Glu505=
XM_024453002.1:c.1616A= XP_024308770.1:p.Glu539=
XM_024453003.1:c.1556A= XP_024308771.1:p.Glu519=
XM_024453004.1:c.1454A= XP_024308772.1:p.Glu485=
XM_024453005.1:c.1436A= XP_024308773.1:p.Glu479=
XM_024453006.1:c.1373A= XP_024308774.1:p.Glu458=
XR_001739705.1:n.3607-567T=
XR_923313.2:n.4043-567T=
NM_000312.4:c.1271A= MANE Select NP_000303.1:p.Glu424=
NM_001375602.1:c.1454A= NP_001362531.1:p.Glu485=
NM_001375603.1:c.1436A= NP_001362532.1:p.Glu479=
NM_001375604.1:c.1334A= NP_001362533.1:p.Glu445=
NM_001375605.1:c.1373A= NP_001362534.1:p.Glu458=
NM_001375606.1:c.1439A= NP_001362535.1:p.Glu480=
NM_001375607.1:c.1457A= NP_001362536.1:p.Glu486=
NM_001375608.1:c.1214A= NP_001362537.1:p.Glu405=
NM_001375609.1:c.1247A= NP_001362538.1:p.Glu416=
NM_001375610.1:c.1265A= NP_001362539.1:p.Glu422=
NM_001375611.1:c.1271A= NP_001362540.1:p.Glu424=
NM_001375613.1:c.1271A= NP_001362542.1:p.Glu424=