Canonical Allele Identifier: CA1286884507
Gene: PROC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127428517C= , CM000664.2:g.127428517C= GRCh38
NC_000002.11:g.128186093C= , CM000664.1:g.128186093C= GRCh37
NC_000002.10:g.127902563C= NCBI36
NG_016323.1:g.15098C= , LRG_599:g.15098C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000234071.8:c.957C= MANE Select ENSP00000234071.4:p.Cys319=
ENST00000234071.7:c.957C= ENSP00000234071.3:p.Cys319=
ENST00000402125.2:c.281C=
ENST00000409048.1:c.1059C= ENSP00000386679.1:p.Cys353=
NM_000312.3:c.957C= , LRG_599t1:c.957C= NP_000303.1:p.Cys319=
XM_005263715.3:c.1140C= XP_005263772.1:p.Cys380=
XM_005263716.3:c.1122C= XP_005263773.1:p.Cys374=
XM_005263717.3:c.1020C= XP_005263774.1:p.Cys340=
XR_923313.1:n.1332-253G=
XM_005263717.4:c.1020C= XP_005263774.1:p.Cys340=
XM_017004505.1:c.1200C= XP_016859994.1:p.Cys400=
XM_024453002.1:c.1302C= XP_024308770.1:p.Cys434=
XM_024453003.1:c.1242C= XP_024308771.1:p.Cys414=
XM_024453004.1:c.1140C= XP_024308772.1:p.Cys380=
XM_024453005.1:c.1122C= XP_024308773.1:p.Cys374=
XM_024453006.1:c.1059C= XP_024308774.1:p.Cys353=
XR_001739705.1:n.3607-253G=
XR_923313.2:n.4043-253G=
NM_000312.4:c.957C= MANE Select NP_000303.1:p.Cys319=
NM_001375602.1:c.1140C= NP_001362531.1:p.Cys380=
NM_001375603.1:c.1122C= NP_001362532.1:p.Cys374=
NM_001375604.1:c.1020C= NP_001362533.1:p.Cys340=
NM_001375605.1:c.1059C= NP_001362534.1:p.Cys353=
NM_001375606.1:c.1125C= NP_001362535.1:p.Cys375=
NM_001375607.1:c.1143C= NP_001362536.1:p.Cys381=
NM_001375608.1:c.900C= NP_001362537.1:p.Cys300=
NM_001375609.1:c.933C= NP_001362538.1:p.Cys311=
NM_001375610.1:c.951C= NP_001362539.1:p.Cys317=
NM_001375611.1:c.957C= NP_001362540.1:p.Cys319=
NM_001375613.1:c.957C= NP_001362542.1:p.Cys319=