Canonical Allele Identifier: CA2586969919
Gene: PROC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127428666del , CM000664.2:g.127428666del GRCh38
NC_000002.11:g.128186242del , CM000664.1:g.128186242del GRCh37
NC_000002.10:g.127902712del NCBI36
NG_016323.1:g.15247del , LRG_599:g.15247del

Transcript Alleles

HGVS Amino-acid Change
ENST00000234071.8:c.1106del MANE Select ENSP00000234071.4:p.Pro369ArgfsTer9
ENST00000234071.7:c.1106del ENSP00000234071.3:p.Pro369ArgfsTer9
ENST00000402125.2:c.430del
ENST00000409048.1:c.1208del ENSP00000386679.1:p.Pro403ArgfsTer9
NM_000312.3:c.1106del , LRG_599t1:c.1106del NP_000303.1:p.Pro369ArgfsTer9
XM_005263715.3:c.1289del XP_005263772.1:p.Pro430ArgfsTer9
XM_005263716.3:c.1271del XP_005263773.1:p.Pro424ArgfsTer9
XM_005263717.3:c.1169del XP_005263774.1:p.Pro390ArgfsTer9
XR_923313.1:n.1332-400del
XM_005263717.4:c.1169del XP_005263774.1:p.Pro390ArgfsTer9
XM_017004505.1:c.1349del XP_016859994.1:p.Pro450ArgfsTer9
XM_024453002.1:c.1451del XP_024308770.1:p.Pro484ArgfsTer9
XM_024453003.1:c.1391del XP_024308771.1:p.Pro464ArgfsTer9
XM_024453004.1:c.1289del XP_024308772.1:p.Pro430ArgfsTer9
XM_024453005.1:c.1271del XP_024308773.1:p.Pro424ArgfsTer9
XM_024453006.1:c.1208del XP_024308774.1:p.Pro403ArgfsTer9
XR_001739705.1:n.3607-400del
XR_923313.2:n.4043-400del
NM_000312.4:c.1106del MANE Select NP_000303.1:p.Pro369ArgfsTer9
NM_001375602.1:c.1289del NP_001362531.1:p.Pro430ArgfsTer9
NM_001375603.1:c.1271del NP_001362532.1:p.Pro424ArgfsTer9
NM_001375604.1:c.1169del NP_001362533.1:p.Pro390ArgfsTer9
NM_001375605.1:c.1208del NP_001362534.1:p.Pro403ArgfsTer9
NM_001375606.1:c.1274del NP_001362535.1:p.Pro425ArgfsTer9
NM_001375607.1:c.1292del NP_001362536.1:p.Pro431ArgfsTer9
NM_001375608.1:c.1049del NP_001362537.1:p.Pro350ArgfsTer9
NM_001375609.1:c.1082del NP_001362538.1:p.Pro361ArgfsTer9
NM_001375610.1:c.1100del NP_001362539.1:p.Pro367ArgfsTer9
NM_001375611.1:c.1106del NP_001362540.1:p.Pro369ArgfsTer9
NM_001375613.1:c.1106del NP_001362542.1:p.Pro369ArgfsTer9