Canonical Allele Identifier: CA2424882612
Gene: OTC HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38403437G= , CM000685.2:g.38403437G= GRCh38
NC_000023.10:g.38262690G= , CM000685.1:g.38262690G= GRCh37
NC_000023.9:g.38147634G= NCBI36
NG_008471.1:g.55955G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000039007.5:c.541-181G= MANE Select ENSP00000039007.4:n.541-181G=
ENST00000643344.1:c.*291-181G= ENSP00000496606.1:n.*291-181G=
ENST00000039007.4:c.541-181G= ENSP00000039007.4:n.541-181G=
ENST00000465127.1:c.172-262684G= ENSP00000417050.1:n.172-262684G=
ENST00000488812.1:n.578-181G=
NM_000531.5:c.541-181G= NP_000522.3:n.541-181G=
XM_017029556.1:c.541-181G= XP_016885045.1:n.541-181G=
NM_000531.6:c.541-181G= MANE Select NP_000522.3:n.541-181G=
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