Canonical Allele Identifier: CA114406
Gene: PROC HGNC NCBI

Linked Data

ClinVar Variation Id: 666
dbSNP Id: rs121918150

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127428560G>A , CM000664.2:g.127428560G>A GRCh38
NC_000002.11:g.128186136G>A , CM000664.1:g.128186136G>A GRCh37
NC_000002.10:g.127902606G>A NCBI36
NG_016323.1:g.15141G>A , LRG_599:g.15141G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000234071.8:c.1000G>A MANE Select ENSP00000234071.4:p.Gly334Ser
ENST00000234071.7:c.1000G>A ENSP00000234071.3:p.Gly334Ser
ENST00000402125.2:n.324G>A
ENST00000409048.1:c.1102G>A ENSP00000386679.1:p.Gly368Ser
NM_000312.3:c.1000G>A , LRG_599t1:c.1000G>A NP_000303.1:p.Gly334Ser
XM_005263715.3:c.1183G>A XP_005263772.1:p.Gly395Ser
XM_005263716.3:c.1165G>A XP_005263773.1:p.Gly389Ser
XM_005263717.3:c.1063G>A XP_005263774.1:p.Gly355Ser
XR_923313.1:n.1332-296C>T
XM_005263717.4:c.1063G>A XP_005263774.1:p.Gly355Ser
XM_017004505.1:c.1243G>A XP_016859994.1:p.Gly415Ser
XM_024453002.1:c.1345G>A XP_024308770.1:p.Gly449Ser
XM_024453003.1:c.1285G>A XP_024308771.1:p.Gly429Ser
XM_024453004.1:c.1183G>A XP_024308772.1:p.Gly395Ser
XM_024453005.1:c.1165G>A XP_024308773.1:p.Gly389Ser
XM_024453006.1:c.1102G>A XP_024308774.1:p.Gly368Ser
XR_001739705.1:n.3607-296C>T
XR_923313.2:n.4043-296C>T
NM_000312.4:c.1000G>A MANE Select NP_000303.1:p.Gly334Ser
NM_001375602.1:c.1183G>A NP_001362531.1:p.Gly395Ser
NM_001375603.1:c.1165G>A NP_001362532.1:p.Gly389Ser
NM_001375604.1:c.1063G>A NP_001362533.1:p.Gly355Ser
NM_001375605.1:c.1102G>A NP_001362534.1:p.Gly368Ser
NM_001375606.1:c.1168G>A NP_001362535.1:p.Gly390Ser
NM_001375607.1:c.1186G>A NP_001362536.1:p.Gly396Ser
NM_001375608.1:c.943G>A NP_001362537.1:p.Gly315Ser
NM_001375609.1:c.976G>A NP_001362538.1:p.Gly326Ser
NM_001375610.1:c.994G>A NP_001362539.1:p.Gly332Ser
NM_001375611.1:c.1000G>A NP_001362540.1:p.Gly334Ser
NM_001375613.1:c.1000G>A NP_001362542.1:p.Gly334Ser