Canonical Allele Identifier: CA348401073
Gene: PROC HGNC NCBI

Linked Data

ClinVar Variation Id: 1068737
ClinVar RCV Id: RCV001380376
dbSNP Id: rs1558715877

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127426110G>A , CM000664.2:g.127426110G>A GRCh38
NC_000002.11:g.128183686G>A , CM000664.1:g.128183686G>A GRCh37
NC_000002.10:g.127900156G>A NCBI36
NG_016323.1:g.12691G>A , LRG_599:g.12691G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000234071.8:c.561G>A MANE Select ENSP00000234071.4:p.Trp187Ter
ENST00000234071.7:c.561G>A ENSP00000234071.3:p.Trp187Ter
ENST00000402125.2:c.121-2247G>A
ENST00000409048.1:c.663G>A ENSP00000386679.1:p.Trp221Ter
ENST00000442644.5:c.504G>A ENSP00000411241.1:p.Trp168Ter
ENST00000464089.1:n.147G>A
NM_000312.3:c.561G>A , LRG_599t1:c.561G>A NP_000303.1:p.Trp187Ter
XM_005263715.3:c.744G>A XP_005263772.1:p.Trp248Ter
XM_005263716.3:c.726G>A XP_005263773.1:p.Trp242Ter
XM_005263717.3:c.624G>A XP_005263774.1:p.Trp208Ter
XM_005263717.4:c.624G>A XP_005263774.1:p.Trp208Ter
XM_017004505.1:c.804G>A XP_016859994.1:p.Trp268Ter
XM_024453002.1:c.906G>A XP_024308770.1:p.Trp302Ter
XM_024453003.1:c.846G>A XP_024308771.1:p.Trp282Ter
XM_024453004.1:c.744G>A XP_024308772.1:p.Trp248Ter
XM_024453005.1:c.726G>A XP_024308773.1:p.Trp242Ter
XM_024453006.1:c.663G>A XP_024308774.1:p.Trp221Ter
XR_923313.2:n.4475C>T
NM_000312.4:c.561G>A MANE Select NP_000303.1:p.Trp187Ter
NM_001375602.1:c.744G>A NP_001362531.1:p.Trp248Ter
NM_001375603.1:c.726G>A NP_001362532.1:p.Trp242Ter
NM_001375604.1:c.624G>A NP_001362533.1:p.Trp208Ter
NM_001375605.1:c.663G>A NP_001362534.1:p.Trp221Ter
NM_001375606.1:c.729G>A NP_001362535.1:p.Trp243Ter
NM_001375607.1:c.747G>A NP_001362536.1:p.Trp249Ter
NM_001375608.1:c.504G>A NP_001362537.1:p.Trp168Ter
NM_001375609.1:c.537G>A NP_001362538.1:p.Trp179Ter
NM_001375610.1:c.555G>A NP_001362539.1:p.Trp185Ter
NM_001375611.1:c.561G>A NP_001362540.1:p.Trp187Ter
NM_001375613.1:c.561G>A NP_001362542.1:p.Trp187Ter