Canonical Allele Identifier: CA515650424

Gene: OTC

Linked Data

• dbSNP Id: rs1423202165
• gnomAD v2: X-38260552-A-G
• gnomAD v4: X-38401299-A-G
• MyVariant Identifiers: chrX:g.38260552A>G (hg19) ; chrX:g.38401299A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38401299A>G , CM000685.2:g.38401299A>G	GRCh38
NC_000023.10:g.38260552A>G , CM000685.1:g.38260552A>G	GRCh37
NC_000023.9:g.38145496A>G	NCBI36
NG_008471.1:g.53817A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000039007.5:c.411A>G MANE Select	ENSP00000039007.4:p.Ala137=
ENST00000643344.1:c.*161A>G	ENSP00000496606.1:n.*161A>G
ENST00000039007.4:c.411A>G	ENSP00000039007.4:p.Ala137=
ENST00000465127.1:c.172-264822A>G	ENSP00000417050.1:n.172-264822A>G
ENST00000488812.1:n.448A>G
NM_000531.5:c.411A>G	NP_000522.3:p.Ala137=
XM_017029556.1:c.411A>G	XP_016885045.1:p.Ala137=
NM_000531.6:c.411A>G MANE Select	NP_000522.3:p.Ala137=