Canonical Allele Identifier: CA413008140

Gene: MAOA

Linked Data

• MyVariant Identifiers: chrX:g.43591052G>A (hg19) ; chrX:g.43731805G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43731805G>A , CM000685.2:g.43731805G>A	GRCh38
NC_000023.10:g.43591052G>A , CM000685.1:g.43591052G>A	GRCh37
NC_000023.9:g.43475996G>A	NCBI36
NG_008957.2:g.80645G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542639.6:c.508G>A	ENSP00000440846.1:p.Val170Ile
ENST00000686683.1:c.217G>A	ENSP00000509063.1:p.Val73Ile
ENST00000686980.1:n.1039G>A
ENST00000688006.1:c.508G>A	ENSP00000510311.1:p.Val170Ile
ENST00000688859.1:n.463G>A
ENST00000689087.1:c.508G>A	ENSP00000508997.1:p.Val170Ile
ENST00000693128.1:c.802G>A	ENSP00000508493.1:p.Val268Ile
ENST00000338702.4:c.907G>A MANE Select	ENSP00000340684.3:p.Val303Ile
ENST00000338702.3:c.907G>A	ENSP00000340684.3:p.Val303Ile
ENST00000542639.5:c.508G>A	ENSP00000440846.1:p.Val170Ile
NM_000240.3:c.907G>A	NP_000231.1:p.Val303Ile
NM_001270458.1:c.508G>A	NP_001257387.1:p.Val170Ile
NM_000240.4:c.907G>A MANE Select	NP_000231.1:p.Val303Ile
NM_001270458.2:c.508G>A	NP_001257387.1:p.Val170Ile