Canonical Allele Identifier: CA2424884267
Gene: OTC HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38408699T= , CM000685.2:g.38408699T= GRCh38
NC_000023.10:g.38267952T= , CM000685.1:g.38267952T= GRCh37
NC_000023.9:g.38152896T= NCBI36
NG_008471.1:g.61217T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000039007.5:c.664-43T= MANE Select ENSP00000039007.4:n.664-43T=
ENST00000643344.1:c.*414-43T= ENSP00000496606.1:n.*414-43T=
ENST00000039007.4:c.664-43T= ENSP00000039007.4:n.664-43T=
ENST00000465127.1:c.172-257422T= ENSP00000417050.1:n.172-257422T=
NM_000531.5:c.664-43T= NP_000522.3:n.664-43T=
XM_017029556.1:c.664-43T= XP_016885045.1:n.664-43T=
NM_000531.6:c.664-43T= MANE Select NP_000522.3:n.664-43T=
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