Canonical Allele Identifier: CA348405930
Gene: PROC HGNC NCBI

Linked Data

dbSNP Id: rs1688691059

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127428692A>G , CM000664.2:g.127428692A>G GRCh38
NC_000002.11:g.128186268A>G , CM000664.1:g.128186268A>G GRCh37
NC_000002.10:g.127902738A>G NCBI36
NG_016323.1:g.15273A>G , LRG_599:g.15273A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000234071.8:c.1132A>G MANE Select ENSP00000234071.4:p.Ser378Gly
ENST00000234071.7:c.1132A>G ENSP00000234071.3:p.Ser378Gly
ENST00000402125.2:c.456A>G
ENST00000409048.1:c.1234A>G ENSP00000386679.1:p.Ser412Gly
NM_000312.3:c.1132A>G , LRG_599t1:c.1132A>G NP_000303.1:p.Ser378Gly
XM_005263715.3:c.1315A>G XP_005263772.1:p.Ser439Gly
XM_005263716.3:c.1297A>G XP_005263773.1:p.Ser433Gly
XM_005263717.3:c.1195A>G XP_005263774.1:p.Ser399Gly
XR_923313.1:n.1332-428T>C
XM_005263717.4:c.1195A>G XP_005263774.1:p.Ser399Gly
XM_017004505.1:c.1375A>G XP_016859994.1:p.Ser459Gly
XM_024453002.1:c.1477A>G XP_024308770.1:p.Ser493Gly
XM_024453003.1:c.1417A>G XP_024308771.1:p.Ser473Gly
XM_024453004.1:c.1315A>G XP_024308772.1:p.Ser439Gly
XM_024453005.1:c.1297A>G XP_024308773.1:p.Ser433Gly
XM_024453006.1:c.1234A>G XP_024308774.1:p.Ser412Gly
XR_001739705.1:n.3607-428T>C
XR_923313.2:n.4043-428T>C
NM_000312.4:c.1132A>G MANE Select NP_000303.1:p.Ser378Gly
NM_001375602.1:c.1315A>G NP_001362531.1:p.Ser439Gly
NM_001375603.1:c.1297A>G NP_001362532.1:p.Ser433Gly
NM_001375604.1:c.1195A>G NP_001362533.1:p.Ser399Gly
NM_001375605.1:c.1234A>G NP_001362534.1:p.Ser412Gly
NM_001375606.1:c.1300A>G NP_001362535.1:p.Ser434Gly
NM_001375607.1:c.1318A>G NP_001362536.1:p.Ser440Gly
NM_001375608.1:c.1075A>G NP_001362537.1:p.Ser359Gly
NM_001375609.1:c.1108A>G NP_001362538.1:p.Ser370Gly
NM_001375610.1:c.1126A>G NP_001362539.1:p.Ser376Gly
NM_001375611.1:c.1132A>G NP_001362540.1:p.Ser378Gly
NM_001375613.1:c.1132A>G NP_001362542.1:p.Ser378Gly