Canonical Allele Identifier: CA348406086
Gene: PROC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127428722G>T , CM000664.2:g.127428722G>T GRCh38
NC_000002.11:g.128186298G>T , CM000664.1:g.128186298G>T GRCh37
NC_000002.10:g.127902768G>T NCBI36
NG_016323.1:g.15303G>T , LRG_599:g.15303G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000234071.8:c.1162G>T MANE Select ENSP00000234071.4:p.Ala388Ser
ENST00000234071.7:c.1162G>T ENSP00000234071.3:p.Ala388Ser
ENST00000402125.2:c.486G>T
ENST00000409048.1:c.1264G>T ENSP00000386679.1:p.Ala422Ser
NM_000312.3:c.1162G>T , LRG_599t1:c.1162G>T NP_000303.1:p.Ala388Ser
XM_005263715.3:c.1345G>T XP_005263772.1:p.Ala449Ser
XM_005263716.3:c.1327G>T XP_005263773.1:p.Ala443Ser
XM_005263717.3:c.1225G>T XP_005263774.1:p.Ala409Ser
XR_923313.1:n.1332-458C>A
XM_005263717.4:c.1225G>T XP_005263774.1:p.Ala409Ser
XM_017004505.1:c.1405G>T XP_016859994.1:p.Ala469Ser
XM_024453002.1:c.1507G>T XP_024308770.1:p.Ala503Ser
XM_024453003.1:c.1447G>T XP_024308771.1:p.Ala483Ser
XM_024453004.1:c.1345G>T XP_024308772.1:p.Ala449Ser
XM_024453005.1:c.1327G>T XP_024308773.1:p.Ala443Ser
XM_024453006.1:c.1264G>T XP_024308774.1:p.Ala422Ser
XR_001739705.1:n.3607-458C>A
XR_923313.2:n.4043-458C>A
NM_000312.4:c.1162G>T MANE Select NP_000303.1:p.Ala388Ser
NM_001375602.1:c.1345G>T NP_001362531.1:p.Ala449Ser
NM_001375603.1:c.1327G>T NP_001362532.1:p.Ala443Ser
NM_001375604.1:c.1225G>T NP_001362533.1:p.Ala409Ser
NM_001375605.1:c.1264G>T NP_001362534.1:p.Ala422Ser
NM_001375606.1:c.1330G>T NP_001362535.1:p.Ala444Ser
NM_001375607.1:c.1348G>T NP_001362536.1:p.Ala450Ser
NM_001375608.1:c.1105G>T NP_001362537.1:p.Ala369Ser
NM_001375609.1:c.1138G>T NP_001362538.1:p.Ala380Ser
NM_001375610.1:c.1156G>T NP_001362539.1:p.Ala386Ser
NM_001375611.1:c.1162G>T NP_001362540.1:p.Ala388Ser
NM_001375613.1:c.1162G>T NP_001362542.1:p.Ala388Ser