Canonical Allele Identifier: CA413008290

Gene: MAOA

Linked Data

• MyVariant Identifiers: chrX:g.43591086T>A (hg19) ; chrX:g.43731839T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43731839T>A , CM000685.2:g.43731839T>A	GRCh38
NC_000023.10:g.43591086T>A , CM000685.1:g.43591086T>A	GRCh37
NC_000023.9:g.43476030T>A	NCBI36
NG_008957.2:g.80679T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542639.6:c.542T>A	ENSP00000440846.1:p.Phe181Tyr
ENST00000686683.1:c.251T>A	ENSP00000509063.1:p.Phe84Tyr
ENST00000686980.1:n.1073T>A
ENST00000688006.1:c.542T>A	ENSP00000510311.1:p.Phe181Tyr
ENST00000688859.1:n.497T>A
ENST00000689087.1:c.542T>A	ENSP00000508997.1:p.Phe181Tyr
ENST00000693128.1:c.836T>A	ENSP00000508493.1:p.Phe279Tyr
ENST00000338702.4:c.941T>A MANE Select	ENSP00000340684.3:p.Phe314Tyr
ENST00000338702.3:c.941T>A	ENSP00000340684.3:p.Phe314Tyr
ENST00000542639.5:c.542T>A	ENSP00000440846.1:p.Phe181Tyr
NM_000240.3:c.941T>A	NP_000231.1:p.Phe314Tyr
NM_001270458.1:c.542T>A	NP_001257387.1:p.Phe181Tyr
NM_000240.4:c.941T>A MANE Select	NP_000231.1:p.Phe314Tyr
NM_001270458.2:c.542T>A	NP_001257387.1:p.Phe181Tyr