Canonical Allele Identifier: CA2424885188
Gene: OTC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38411833A= , CM000685.2:g.38411833A= GRCh38
NC_000023.10:g.38271086A= , CM000685.1:g.38271086A= GRCh37
NC_000023.9:g.38156030A= NCBI36
NG_008471.1:g.64351A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000039007.5:c.868-29A= MANE Select ENSP00000039007.4:n.868-29A=
ENST00000643344.1:c.*618-29A= ENSP00000496606.1:n.*618-29A=
ENST00000039007.4:c.868-29A= ENSP00000039007.4:n.868-29A=
ENST00000465127.1:c.172-254288A= ENSP00000417050.1:n.172-254288A=
NM_000531.5:c.868-29A= NP_000522.3:n.868-29A=
XM_017029556.1:c.908A= XP_016885045.1:p.Gln303=
NM_000531.6:c.868-29A= MANE Select NP_000522.3:n.868-29A=