Canonical Allele Identifier: CA349279
Gene: PROC HGNC NCBI

Linked Data

ClinVar Variation Id: 219771
ClinVar RCV Id: RCV000205093
dbSNP Id: rs151319700

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127428859C>T , CM000664.2:g.127428859C>T GRCh38
NC_000002.11:g.128186435C>T , CM000664.1:g.128186435C>T GRCh37
NC_000002.10:g.127902905C>T NCBI36
NG_016323.1:g.15440C>T , LRG_599:g.15440C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000234071.8:c.1299C>T MANE Select ENSP00000234071.4:p.Gly433=
ENST00000234071.7:c.1299C>T ENSP00000234071.3:p.Gly433=
ENST00000402125.2:c.623C>T
ENST00000409048.1:c.1401C>T ENSP00000386679.1:p.Gly467=
NM_000312.3:c.1299C>T , LRG_599t1:c.1299C>T NP_000303.1:p.Gly433=
XM_005263715.3:c.1482C>T XP_005263772.1:p.Gly494=
XM_005263716.3:c.1464C>T XP_005263773.1:p.Gly488=
XM_005263717.3:c.1362C>T XP_005263774.1:p.Gly454=
XR_923313.1:n.1332-595G>A
XM_005263717.4:c.1362C>T XP_005263774.1:p.Gly454=
XM_017004505.1:c.1542C>T XP_016859994.1:p.Gly514=
XM_024453002.1:c.1644C>T XP_024308770.1:p.Gly548=
XM_024453003.1:c.1584C>T XP_024308771.1:p.Gly528=
XM_024453004.1:c.1482C>T XP_024308772.1:p.Gly494=
XM_024453005.1:c.1464C>T XP_024308773.1:p.Gly488=
XM_024453006.1:c.1401C>T XP_024308774.1:p.Gly467=
XR_001739705.1:n.3607-595G>A
XR_923313.2:n.4043-595G>A
NM_000312.4:c.1299C>T MANE Select NP_000303.1:p.Gly433=
NM_001375602.1:c.1482C>T NP_001362531.1:p.Gly494=
NM_001375603.1:c.1464C>T NP_001362532.1:p.Gly488=
NM_001375604.1:c.1362C>T NP_001362533.1:p.Gly454=
NM_001375605.1:c.1401C>T NP_001362534.1:p.Gly467=
NM_001375606.1:c.1467C>T NP_001362535.1:p.Gly489=
NM_001375607.1:c.1485C>T NP_001362536.1:p.Gly495=
NM_001375608.1:c.1242C>T NP_001362537.1:p.Gly414=
NM_001375609.1:c.1275C>T NP_001362538.1:p.Gly425=
NM_001375610.1:c.1293C>T NP_001362539.1:p.Gly431=
NM_001375611.1:c.1299C>T NP_001362540.1:p.Gly433=
NM_001375613.1:c.1299C>T NP_001362542.1:p.Gly433=