Canonical Allele Identifier: CA2579584750
Gene: OTC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38369901del , CM000685.2:g.38369901del GRCh38
NC_000023.10:g.38229154del , CM000685.1:g.38229154del GRCh37
NC_000023.9:g.38114098del NCBI36
NG_008471.1:g.22419del

Transcript Alleles

HGVS Amino-acid change
ENST00000039007.5:c.298+24del MANE Select ENSP00000039007.4:n.298+24del
ENST00000643344.1:c.298+24del ENSP00000496606.1:n.298+24del
ENST00000039007.4:c.298+24del ENSP00000039007.4:n.298+24del
ENST00000465127.1:c.172-296220del ENSP00000417050.1:n.172-296220del
ENST00000488812.1:n.353+61del
NM_000531.5:c.298+24del NP_000522.3:n.298+24del
XM_017029556.1:c.298+24del XP_016885045.1:n.298+24del
NM_000531.6:c.298+24del MANE Select NP_000522.3:n.298+24del