Canonical Allele Identifier: CA412722878
Gene: OTC HGNC NCBI

Linked Data

gnomAD v4: X-38408942-A-G
MyVariant Identifiers: chrX:g.38268195A>G (hg19) chrX:g.38408942A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38408942A>G , CM000685.2:g.38408942A>G GRCh38
NC_000023.10:g.38268195A>G , CM000685.1:g.38268195A>G GRCh37
NC_000023.9:g.38153139A>G NCBI36
NG_008471.1:g.61460A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000039007.5:c.784A>G MANE Select ENSP00000039007.4:p.Thr262Ala
ENST00000643344.1:c.*534A>G ENSP00000496606.1:n.*534A>G
ENST00000039007.4:c.784A>G ENSP00000039007.4:p.Thr262Ala
ENST00000465127.1:c.172-257179A>G ENSP00000417050.1:n.172-257179A>G
NM_000531.5:c.784A>G NP_000522.3:p.Thr262Ala
XM_017029556.1:c.784A>G XP_016885045.1:p.Thr262Ala
NM_000531.6:c.784A>G MANE Select NP_000522.3:p.Thr262Ala
Search 100 bp 5'
Search 100 bp 3'