Canonical Allele Identifier: CA412725348
Gene: OTC HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.38262905G>A (hg19) chrX:g.38403652G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38403652G>A , CM000685.2:g.38403652G>A GRCh38
NC_000023.10:g.38262905G>A , CM000685.1:g.38262905G>A GRCh37
NC_000023.9:g.38147849G>A NCBI36
NG_008471.1:g.56170G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000039007.5:c.575G>A MANE Select ENSP00000039007.4:p.Ser192Asn
ENST00000643344.1:c.*325G>A ENSP00000496606.1:n.*325G>A
ENST00000039007.4:c.575G>A ENSP00000039007.4:p.Ser192Asn
ENST00000465127.1:c.172-262469G>A ENSP00000417050.1:n.172-262469G>A
ENST00000488812.1:n.612G>A
NM_000531.5:c.575G>A NP_000522.3:p.Ser192Asn
XM_017029556.1:c.575G>A XP_016885045.1:p.Ser192Asn
NM_000531.6:c.575G>A MANE Select NP_000522.3:p.Ser192Asn
Search 100 bp 5'
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