Canonical Allele Identifier: CA2693443216
Gene: OTC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38408985del , CM000685.2:g.38408985del GRCh38
NC_000023.10:g.38268238del , CM000685.1:g.38268238del GRCh37
NC_000023.9:g.38153182del NCBI36
NG_008471.1:g.61503del

Transcript Alleles

HGVS Amino-acid Change
ENST00000039007.5:c.827del MANE Select ENSP00000039007.4:p.Lys276SerfsTer13
ENST00000643344.1:c.*577del ENSP00000496606.1:n.*577del
ENST00000039007.4:c.827del ENSP00000039007.4:p.Lys276SerfsTer13
ENST00000465127.1:c.172-257136del ENSP00000417050.1:n.172-257136del
NM_000531.5:c.827del NP_000522.3:p.Lys276SerfsTer13
XM_017029556.1:c.827del XP_016885045.1:p.Lys276SerfsTer13
NM_000531.6:c.827del MANE Select NP_000522.3:p.Lys276SerfsTer13