Canonical Allele Identifier: CA2424884391
Gene: OTC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38409020A= , CM000685.2:g.38409020A= GRCh38
NC_000023.10:g.38268273A= , CM000685.1:g.38268273A= GRCh37
NC_000023.9:g.38153217A= NCBI36
NG_008471.1:g.61538A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000039007.5:c.862A= MANE Select ENSP00000039007.4:p.Met288=
ENST00000643344.1:c.*612A= ENSP00000496606.1:n.*612A=
ENST00000039007.4:c.862A= ENSP00000039007.4:p.Met288=
ENST00000465127.1:c.172-257101A= ENSP00000417050.1:n.172-257101A=
NM_000531.5:c.862A= NP_000522.3:p.Met288=
XM_017029556.1:c.862A= XP_016885045.1:p.Met288=
NM_000531.6:c.862A= MANE Select NP_000522.3:p.Met288=