Canonical Allele Identifier: CA2424884411
Gene: OTC HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38409088T= , CM000685.2:g.38409088T= GRCh38
NC_000023.10:g.38268341T= , CM000685.1:g.38268341T= GRCh37
NC_000023.9:g.38153285T= NCBI36
NG_008471.1:g.61606T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000039007.5:c.867+63T= MANE Select ENSP00000039007.4:n.867+63T=
ENST00000643344.1:c.*617+63T= ENSP00000496606.1:n.*617+63T=
ENST00000039007.4:c.867+63T= ENSP00000039007.4:n.867+63T=
ENST00000465127.1:c.172-257033T= ENSP00000417050.1:n.172-257033T=
NM_000531.5:c.867+63T= NP_000522.3:n.867+63T=
XM_017029556.1:c.867+63T= XP_016885045.1:n.867+63T=
NM_000531.6:c.867+63T= MANE Select NP_000522.3:n.867+63T=
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