Canonical Allele Identifier: CA413007487

Gene: MAOA

Linked Data

• MyVariant Identifiers: chrX:g.43590959G>A (hg19) ; chrX:g.43731712G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43731712G>A , CM000685.2:g.43731712G>A	GRCh38
NC_000023.10:g.43590959G>A , CM000685.1:g.43590959G>A	GRCh37
NC_000023.9:g.43475903G>A	NCBI36
NG_008957.2:g.80552G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542639.6:c.415G>A	ENSP00000440846.1:p.Ala139Thr
ENST00000686683.1:c.124G>A	ENSP00000509063.1:p.Ala42Thr
ENST00000686980.1:n.946G>A
ENST00000688006.1:c.415G>A	ENSP00000510311.1:p.Ala139Thr
ENST00000688859.1:n.370G>A
ENST00000689087.1:c.415G>A	ENSP00000508997.1:p.Ala139Thr
ENST00000693128.1:c.709G>A	ENSP00000508493.1:p.Ala237Thr
ENST00000338702.4:c.814G>A MANE Select	ENSP00000340684.3:p.Ala272Thr
ENST00000338702.3:c.814G>A	ENSP00000340684.3:p.Ala272Thr
ENST00000542639.5:c.415G>A	ENSP00000440846.1:p.Ala139Thr
NM_000240.3:c.814G>A	NP_000231.1:p.Ala272Thr
NM_001270458.1:c.415G>A	NP_001257387.1:p.Ala139Thr
NM_000240.4:c.814G>A MANE Select	NP_000231.1:p.Ala272Thr
NM_001270458.2:c.415G>A	NP_001257387.1:p.Ala139Thr