Canonical Allele Identifier: CA412716942
Gene: OTC HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.38229090T>A (hg19) chrX:g.38369837T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38369837T>A , CM000685.2:g.38369837T>A GRCh38
NC_000023.10:g.38229090T>A , CM000685.1:g.38229090T>A GRCh37
NC_000023.9:g.38114034T>A NCBI36
NG_008471.1:g.22355T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000039007.5:c.258T>A MANE Select ENSP00000039007.4:p.Phe86Leu
ENST00000643344.1:c.258T>A ENSP00000496606.1:p.Phe86Leu
ENST00000039007.4:c.258T>A ENSP00000039007.4:p.Phe86Leu
ENST00000465127.1:c.172-296284T>A ENSP00000417050.1:n.172-296284T>A
ENST00000488812.1:n.350T>A
NM_000531.5:c.258T>A NP_000522.3:p.Phe86Leu
XM_017029556.1:c.258T>A XP_016885045.1:p.Phe86Leu
NM_000531.6:c.258T>A MANE Select NP_000522.3:p.Phe86Leu
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