Canonical Allele Identifier: CA2693442240
Gene: OTC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38367357del , CM000685.2:g.38367357del GRCh38
NC_000023.10:g.38226610del , CM000685.1:g.38226610del GRCh37
NC_000023.9:g.38111554del NCBI36
NG_008471.1:g.19875del

Transcript Alleles

HGVS Amino-acid change
ENST00000039007.5:c.144del MANE Select ENSP00000039007.4:p.Phe48LeufsTer16
ENST00000643344.1:c.144del ENSP00000496606.1:p.Phe48LeufsTer16
ENST00000039007.4:c.144del ENSP00000039007.4:p.Phe48LeufsTer16
ENST00000465127.1:c.172-298764del ENSP00000417050.1:n.172-298764del
ENST00000488812.1:n.236del
NM_000531.5:c.144del NP_000522.3:p.Phe48LeufsTer16
XM_017029556.1:c.144del XP_016885045.1:p.Phe48LeufsTer16
NM_000531.6:c.144del MANE Select NP_000522.3:p.Phe48LeufsTer16