Canonical Allele Identifier: CA2579584747
Gene: OTC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38369885del , CM000685.2:g.38369885del GRCh38
NC_000023.10:g.38229138del , CM000685.1:g.38229138del GRCh37
NC_000023.9:g.38114082del NCBI36
NG_008471.1:g.22403del

Transcript Alleles

HGVS Amino-acid change
ENST00000039007.5:c.298+8del MANE Select ENSP00000039007.4:n.298+8del
ENST00000643344.1:c.298+8del ENSP00000496606.1:n.298+8del
ENST00000039007.4:c.298+8del ENSP00000039007.4:n.298+8del
ENST00000465127.1:c.172-296236del ENSP00000417050.1:n.172-296236del
ENST00000488812.1:n.353+45del
NM_000531.5:c.298+8del NP_000522.3:n.298+8del
XM_017029556.1:c.298+8del XP_016885045.1:n.298+8del
NM_000531.6:c.298+8del MANE Select NP_000522.3:n.298+8del