Canonical Allele Identifier: CA412716938
Gene: OTC HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.38229089T>A (hg19) chrX:g.38369836T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38369836T>A , CM000685.2:g.38369836T>A GRCh38
NC_000023.10:g.38229089T>A , CM000685.1:g.38229089T>A GRCh37
NC_000023.9:g.38114033T>A NCBI36
NG_008471.1:g.22354T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000039007.5:c.257T>A MANE Select ENSP00000039007.4:p.Phe86Tyr
ENST00000643344.1:c.257T>A ENSP00000496606.1:p.Phe86Tyr
ENST00000039007.4:c.257T>A ENSP00000039007.4:p.Phe86Tyr
ENST00000465127.1:c.172-296285T>A ENSP00000417050.1:n.172-296285T>A
ENST00000488812.1:n.349T>A
NM_000531.5:c.257T>A NP_000522.3:p.Phe86Tyr
XM_017029556.1:c.257T>A XP_016885045.1:p.Phe86Tyr
NM_000531.6:c.257T>A MANE Select NP_000522.3:p.Phe86Tyr
Search 100 bp 5'
Search 100 bp 3'