Canonical Allele Identifier: CA2586969912
Gene: PROC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127428524del , CM000664.2:g.127428524del GRCh38
NC_000002.11:g.128186100del , CM000664.1:g.128186100del GRCh37
NC_000002.10:g.127902570del NCBI36
NG_016323.1:g.15105del , LRG_599:g.15105del

Transcript Alleles

HGVS Amino-acid Change
ENST00000234071.8:c.964del MANE Select ENSP00000234071.4:p.Asp322ThrfsTer18
ENST00000234071.7:c.964del ENSP00000234071.3:p.Asp322ThrfsTer18
ENST00000402125.2:c.288del
ENST00000409048.1:c.1066del ENSP00000386679.1:p.Asp356ThrfsTer18
NM_000312.3:c.964del , LRG_599t1:c.964del NP_000303.1:p.Asp322ThrfsTer18
XM_005263715.3:c.1147del XP_005263772.1:p.Asp383ThrfsTer18
XM_005263716.3:c.1129del XP_005263773.1:p.Asp377ThrfsTer18
XM_005263717.3:c.1027del XP_005263774.1:p.Asp343ThrfsTer18
XR_923313.1:n.1332-259del
XM_005263717.4:c.1027del XP_005263774.1:p.Asp343ThrfsTer18
XM_017004505.1:c.1207del XP_016859994.1:p.Asp403ThrfsTer18
XM_024453002.1:c.1309del XP_024308770.1:p.Asp437ThrfsTer18
XM_024453003.1:c.1249del XP_024308771.1:p.Asp417ThrfsTer18
XM_024453004.1:c.1147del XP_024308772.1:p.Asp383ThrfsTer18
XM_024453005.1:c.1129del XP_024308773.1:p.Asp377ThrfsTer18
XM_024453006.1:c.1066del XP_024308774.1:p.Asp356ThrfsTer18
XR_001739705.1:n.3607-259del
XR_923313.2:n.4043-259del
NM_000312.4:c.964del MANE Select NP_000303.1:p.Asp322ThrfsTer18
NM_001375602.1:c.1147del NP_001362531.1:p.Asp383ThrfsTer18
NM_001375603.1:c.1129del NP_001362532.1:p.Asp377ThrfsTer18
NM_001375604.1:c.1027del NP_001362533.1:p.Asp343ThrfsTer18
NM_001375605.1:c.1066del NP_001362534.1:p.Asp356ThrfsTer18
NM_001375606.1:c.1132del NP_001362535.1:p.Asp378ThrfsTer18
NM_001375607.1:c.1150del NP_001362536.1:p.Asp384ThrfsTer18
NM_001375608.1:c.907del NP_001362537.1:p.Asp303ThrfsTer18
NM_001375609.1:c.940del NP_001362538.1:p.Asp314ThrfsTer18
NM_001375610.1:c.958del NP_001362539.1:p.Asp320ThrfsTer18
NM_001375611.1:c.964del NP_001362540.1:p.Asp322ThrfsTer18
NM_001375613.1:c.964del NP_001362542.1:p.Asp322ThrfsTer18