Canonical Allele Identifier: CA1859534
Gene: PROC HGNC NCBI

Linked Data

dbSNP Id: rs769277939

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127428723C>G , CM000664.2:g.127428723C>G GRCh38
NC_000002.11:g.128186299C>G , CM000664.1:g.128186299C>G GRCh37
NC_000002.10:g.127902769C>G NCBI36
NG_016323.1:g.15304C>G , LRG_599:g.15304C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000234071.8:c.1163C>G MANE Select ENSP00000234071.4:p.Ala388Gly
ENST00000234071.7:c.1163C>G ENSP00000234071.3:p.Ala388Gly
ENST00000402125.2:c.487C>G
ENST00000409048.1:c.1265C>G ENSP00000386679.1:p.Ala422Gly
NM_000312.3:c.1163C>G , LRG_599t1:c.1163C>G NP_000303.1:p.Ala388Gly
XM_005263715.3:c.1346C>G XP_005263772.1:p.Ala449Gly
XM_005263716.3:c.1328C>G XP_005263773.1:p.Ala443Gly
XM_005263717.3:c.1226C>G XP_005263774.1:p.Ala409Gly
XR_923313.1:n.1332-459G>C
XM_005263717.4:c.1226C>G XP_005263774.1:p.Ala409Gly
XM_017004505.1:c.1406C>G XP_016859994.1:p.Ala469Gly
XM_024453002.1:c.1508C>G XP_024308770.1:p.Ala503Gly
XM_024453003.1:c.1448C>G XP_024308771.1:p.Ala483Gly
XM_024453004.1:c.1346C>G XP_024308772.1:p.Ala449Gly
XM_024453005.1:c.1328C>G XP_024308773.1:p.Ala443Gly
XM_024453006.1:c.1265C>G XP_024308774.1:p.Ala422Gly
XR_001739705.1:n.3607-459G>C
XR_923313.2:n.4043-459G>C
NM_000312.4:c.1163C>G MANE Select NP_000303.1:p.Ala388Gly
NM_001375602.1:c.1346C>G NP_001362531.1:p.Ala449Gly
NM_001375603.1:c.1328C>G NP_001362532.1:p.Ala443Gly
NM_001375604.1:c.1226C>G NP_001362533.1:p.Ala409Gly
NM_001375605.1:c.1265C>G NP_001362534.1:p.Ala422Gly
NM_001375606.1:c.1331C>G NP_001362535.1:p.Ala444Gly
NM_001375607.1:c.1349C>G NP_001362536.1:p.Ala450Gly
NM_001375608.1:c.1106C>G NP_001362537.1:p.Ala369Gly
NM_001375609.1:c.1139C>G NP_001362538.1:p.Ala380Gly
NM_001375610.1:c.1157C>G NP_001362539.1:p.Ala386Gly
NM_001375611.1:c.1163C>G NP_001362540.1:p.Ala388Gly
NM_001375613.1:c.1163C>G NP_001362542.1:p.Ala388Gly