Canonical Allele Identifier: CA224824
Gene: OTC HGNC NCBI

Linked Data

ClinVar Variation Id: 97351
ClinVar RCV Id: RCV000083599
dbSNP Id: rs72558463
MyVariant Identifiers: chrX:g.38271151C>T (hg19) chrX:g.38411898C>T (hg38)
PubMed: PMID:8956038
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38411898C>T , CM000685.2:g.38411898C>T GRCh38
NC_000023.10:g.38271151C>T , CM000685.1:g.38271151C>T GRCh37
NC_000023.9:g.38156095C>T NCBI36
NG_008471.1:g.64416C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000039007.5:c.904C>T MANE Select ENSP00000039007.4:p.His302Tyr
ENST00000643344.1:c.*654C>T ENSP00000496606.1:n.*654C>T
ENST00000039007.4:c.904C>T ENSP00000039007.4:p.His302Tyr
ENST00000465127.1:c.172-254223C>T ENSP00000417050.1:n.172-254223C>T
NM_000531.5:c.904C>T NP_000522.3:p.His302Tyr
NM_000531.6:c.904C>T MANE Select NP_000522.3:p.His302Tyr
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