Canonical Allele Identifier: CA515642277
Gene: OTC HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.38268203T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38408950T>A , CM000685.2:g.38408950T>A GRCh38
NC_000023.10:g.38268203T>A , CM000685.1:g.38268203T>A GRCh37
NC_000023.9:g.38153147T>A NCBI36
NG_008471.1:g.61468T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000039007.5:c.792T>A MANE Select ENSP00000039007.4:p.Thr264=
ENST00000643344.1:c.*542T>A ENSP00000496606.1:n.*542T>A
ENST00000039007.4:c.792T>A ENSP00000039007.4:p.Thr264=
ENST00000465127.1:c.172-257171T>A ENSP00000417050.1:n.172-257171T>A
NM_000531.5:c.792T>A NP_000522.3:p.Thr264=
XM_017029556.1:c.792T>A XP_016885045.1:p.Thr264=
NM_000531.6:c.792T>A MANE Select NP_000522.3:p.Thr264=