Canonical Allele Identifier: CA515642286

Gene: OTC

Linked Data

• MyVariant Identifiers: chrX:g.38268209A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38408956A>T , CM000685.2:g.38408956A>T	GRCh38
NC_000023.10:g.38268209A>T , CM000685.1:g.38268209A>T	GRCh37
NC_000023.9:g.38153153A>T	NCBI36
NG_008471.1:g.61474A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000039007.5:c.798A>T MANE Select	ENSP00000039007.4:p.Ile266=
ENST00000643344.1:c.*548A>T	ENSP00000496606.1:n.*548A>T
ENST00000039007.4:c.798A>T	ENSP00000039007.4:p.Ile266=
ENST00000465127.1:c.172-257165A>T	ENSP00000417050.1:n.172-257165A>T
NM_000531.5:c.798A>T	NP_000522.3:p.Ile266=
XM_017029556.1:c.798A>T	XP_016885045.1:p.Ile266=
NM_000531.6:c.798A>T MANE Select	NP_000522.3:p.Ile266=