Canonical Allele Identifier: CA1036160240
Gene: PROC HGNC NCBI

Linked Data

dbSNP Id: rs1688652541

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127428243del , CM000664.2:g.127428243del GRCh38
NC_000002.11:g.128185819del , CM000664.1:g.128185819del GRCh37
NC_000002.10:g.127902289del NCBI36
NG_016323.1:g.14824del , LRG_599:g.14824del

Transcript Alleles

HGVS Amino-acid Change
ENST00000234071.8:c.797-114del MANE Select ENSP00000234071.4:n.797-114del
ENST00000234071.7:c.797-114del ENSP00000234071.3:n.797-114del
ENST00000402125.2:c.121-114del
ENST00000409048.1:c.899-114del ENSP00000386679.1:n.899-114del
NM_000312.3:c.797-114del , LRG_599t1:c.797-114del NP_000303.1:n.797-114del
XM_005263715.3:c.980-114del XP_005263772.1:n.980-114del
XM_005263716.3:c.962-114del XP_005263773.1:n.962-114del
XM_005263717.3:c.860-114del XP_005263774.1:n.860-114del
XR_923313.1:n.1354del
XM_005263717.4:c.860-114del XP_005263774.1:n.860-114del
XM_017004505.1:c.1040-114del XP_016859994.1:n.1040-114del
XM_024453002.1:c.1142-114del XP_024308770.1:n.1142-114del
XM_024453003.1:c.1082-114del XP_024308771.1:n.1082-114del
XM_024453004.1:c.980-114del XP_024308772.1:n.980-114del
XM_024453005.1:c.962-114del XP_024308773.1:n.962-114del
XM_024453006.1:c.899-114del XP_024308774.1:n.899-114del
XR_001739705.1:n.3629del
XR_923313.2:n.4065del
NM_000312.4:c.797-114del MANE Select NP_000303.1:n.797-114del
NM_001375602.1:c.980-114del NP_001362531.1:n.980-114del
NM_001375603.1:c.962-114del NP_001362532.1:n.962-114del
NM_001375604.1:c.860-114del NP_001362533.1:n.860-114del
NM_001375605.1:c.899-114del NP_001362534.1:n.899-114del
NM_001375606.1:c.965-114del NP_001362535.1:n.965-114del
NM_001375607.1:c.983-114del NP_001362536.1:n.983-114del
NM_001375608.1:c.740-114del NP_001362537.1:n.740-114del
NM_001375609.1:c.773-114del NP_001362538.1:n.773-114del
NM_001375610.1:c.791-114del NP_001362539.1:n.791-114del
NM_001375611.1:c.797-114del NP_001362540.1:n.797-114del
NM_001375613.1:c.797-114del NP_001362542.1:n.797-114del