Canonical Allele Identifier: CA412722488
Gene: OTC HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.38268157A>C (hg19) chrX:g.38408904A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38408904A>C , CM000685.2:g.38408904A>C GRCh38
NC_000023.10:g.38268157A>C , CM000685.1:g.38268157A>C GRCh37
NC_000023.9:g.38153101A>C NCBI36
NG_008471.1:g.61422A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000039007.5:c.746A>C MANE Select ENSP00000039007.4:p.Asp249Ala
ENST00000643344.1:c.*496A>C ENSP00000496606.1:n.*496A>C
ENST00000039007.4:c.746A>C ENSP00000039007.4:p.Asp249Ala
ENST00000465127.1:c.172-257217A>C ENSP00000417050.1:n.172-257217A>C
NM_000531.5:c.746A>C NP_000522.3:p.Asp249Ala
XM_017029556.1:c.746A>C XP_016885045.1:p.Asp249Ala
NM_000531.6:c.746A>C MANE Select NP_000522.3:p.Asp249Ala
Search 100 bp 5'
Search 100 bp 3'