Canonical Allele Identifier: CA348401296
Gene: PROC HGNC NCBI

Linked Data

ClinVar Variation Id: 839161
dbSNP Id: rs1456533664

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127426144C>T , CM000664.2:g.127426144C>T GRCh38
NC_000002.11:g.128183720C>T , CM000664.1:g.128183720C>T GRCh37
NC_000002.10:g.127900190C>T NCBI36
NG_016323.1:g.12725C>T , LRG_599:g.12725C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000234071.8:c.595C>T MANE Select ENSP00000234071.4:p.Arg199Ter
ENST00000234071.7:c.595C>T ENSP00000234071.3:p.Arg199Ter
ENST00000402125.2:c.121-2213C>T
ENST00000409048.1:c.697C>T ENSP00000386679.1:p.Arg233Ter
ENST00000464089.1:n.181C>T
NM_000312.3:c.595C>T , LRG_599t1:c.595C>T NP_000303.1:p.Arg199Ter
XM_005263715.3:c.778C>T XP_005263772.1:p.Arg260Ter
XM_005263716.3:c.760C>T XP_005263773.1:p.Arg254Ter
XM_005263717.3:c.658C>T XP_005263774.1:p.Arg220Ter
XM_005263717.4:c.658C>T XP_005263774.1:p.Arg220Ter
XM_017004505.1:c.838C>T XP_016859994.1:p.Arg280Ter
XM_024453002.1:c.940C>T XP_024308770.1:p.Arg314Ter
XM_024453003.1:c.880C>T XP_024308771.1:p.Arg294Ter
XM_024453004.1:c.778C>T XP_024308772.1:p.Arg260Ter
XM_024453005.1:c.760C>T XP_024308773.1:p.Arg254Ter
XM_024453006.1:c.697C>T XP_024308774.1:p.Arg233Ter
XR_923313.2:n.4441G>A
NM_000312.4:c.595C>T MANE Select NP_000303.1:p.Arg199Ter
NM_001375602.1:c.778C>T NP_001362531.1:p.Arg260Ter
NM_001375603.1:c.760C>T NP_001362532.1:p.Arg254Ter
NM_001375604.1:c.658C>T NP_001362533.1:p.Arg220Ter
NM_001375605.1:c.697C>T NP_001362534.1:p.Arg233Ter
NM_001375606.1:c.763C>T NP_001362535.1:p.Arg255Ter
NM_001375607.1:c.781C>T NP_001362536.1:p.Arg261Ter
NM_001375608.1:c.538C>T NP_001362537.1:p.Arg180Ter
NM_001375609.1:c.571C>T NP_001362538.1:p.Arg191Ter
NM_001375610.1:c.589C>T NP_001362539.1:p.Arg197Ter
NM_001375611.1:c.595C>T NP_001362540.1:p.Arg199Ter
NM_001375613.1:c.595C>T NP_001362542.1:p.Arg199Ter