Canonical Allele Identifier: CA2579584861
Gene: OTC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38408718del , CM000685.2:g.38408718del GRCh38
NC_000023.10:g.38267971del , CM000685.1:g.38267971del GRCh37
NC_000023.9:g.38152915del NCBI36
NG_008471.1:g.61236del

Transcript Alleles

HGVS Amino-acid change
ENST00000039007.5:c.664-24del MANE Select ENSP00000039007.4:n.664-24del
ENST00000643344.1:c.*414-24del ENSP00000496606.1:n.*414-24del
ENST00000039007.4:c.664-24del ENSP00000039007.4:n.664-24del
ENST00000465127.1:c.172-257403del ENSP00000417050.1:n.172-257403del
NM_000531.5:c.664-24del NP_000522.3:n.664-24del
XM_017029556.1:c.664-24del XP_016885045.1:n.664-24del
NM_000531.6:c.664-24del MANE Select NP_000522.3:n.664-24del