Canonical Allele Identifier: CA2579584745
Gene: OTC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38369881del , CM000685.2:g.38369881del GRCh38
NC_000023.10:g.38229134del , CM000685.1:g.38229134del GRCh37
NC_000023.9:g.38114078del NCBI36
NG_008471.1:g.22399del

Transcript Alleles

HGVS Amino-acid change
ENST00000039007.5:c.298+4del MANE Select ENSP00000039007.4:n.298+4del
ENST00000643344.1:c.298+4del ENSP00000496606.1:n.298+4del
ENST00000039007.4:c.298+4del ENSP00000039007.4:n.298+4del
ENST00000465127.1:c.172-296240del ENSP00000417050.1:n.172-296240del
ENST00000488812.1:n.353+41del
NM_000531.5:c.298+4del NP_000522.3:n.298+4del
XM_017029556.1:c.298+4del XP_016885045.1:n.298+4del
NM_000531.6:c.298+4del MANE Select NP_000522.3:n.298+4del