Canonical Allele Identifier: CA2579584830
Gene: OTC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38403554del , CM000685.2:g.38403554del GRCh38
NC_000023.10:g.38262807del , CM000685.1:g.38262807del GRCh37
NC_000023.9:g.38147751del NCBI36
NG_008471.1:g.56072del

Transcript Alleles

HGVS Amino-acid Change
ENST00000039007.5:c.541-64del MANE Select ENSP00000039007.4:n.541-64del
ENST00000643344.1:c.*291-64del ENSP00000496606.1:n.*291-64del
ENST00000039007.4:c.541-64del ENSP00000039007.4:n.541-64del
ENST00000465127.1:c.172-262567del ENSP00000417050.1:n.172-262567del
ENST00000488812.1:n.578-64del
NM_000531.5:c.541-64del NP_000522.3:n.541-64del
XM_017029556.1:c.541-64del XP_016885045.1:n.541-64del
NM_000531.6:c.541-64del MANE Select NP_000522.3:n.541-64del