Canonical Allele Identifier: CA2424884360
Gene: OTC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38408946A= , CM000685.2:g.38408946A= GRCh38
NC_000023.10:g.38268199A= , CM000685.1:g.38268199A= GRCh37
NC_000023.9:g.38153143A= NCBI36
NG_008471.1:g.61464A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000039007.5:c.788A= MANE Select ENSP00000039007.4:p.Asp263=
ENST00000643344.1:c.*538A= ENSP00000496606.1:n.*538A=
ENST00000039007.4:c.788A= ENSP00000039007.4:p.Asp263=
ENST00000465127.1:c.172-257175A= ENSP00000417050.1:n.172-257175A=
NM_000531.5:c.788A= NP_000522.3:p.Asp263=
XM_017029556.1:c.788A= XP_016885045.1:p.Asp263=
NM_000531.6:c.788A= MANE Select NP_000522.3:p.Asp263=