Canonical Allele Identifier: CA10390845

Gene: MAOA

Linked Data

• ClinVar Variation Id: 732079
• ClinVar RCV Id: RCV000907153
• dbSNP Id: rs751223564
• ExAC: X:43590961 G / A
• gnomAD v2: X-43590961-G-A
• gnomAD v3: X-43731714-G-A
• gnomAD v4: X-43731714-G-A
• MyVariant Identifiers: chrX:g.43590961G>A (hg19) ; chrX:g.43731714G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43731714G>A , CM000685.2:g.43731714G>A	GRCh38
NC_000023.10:g.43590961G>A , CM000685.1:g.43590961G>A	GRCh37
NC_000023.9:g.43475905G>A	NCBI36
NG_008957.2:g.80554G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542639.6:c.417G>A	ENSP00000440846.1:p.Ala139=
ENST00000686683.1:c.126G>A	ENSP00000509063.1:p.Ala42=
ENST00000686980.1:n.948G>A
ENST00000688006.1:c.417G>A	ENSP00000510311.1:p.Ala139=
ENST00000688859.1:n.372G>A
ENST00000689087.1:c.417G>A	ENSP00000508997.1:p.Ala139=
ENST00000693128.1:c.711G>A	ENSP00000508493.1:p.Ala237=
ENST00000338702.4:c.816G>A MANE Select	ENSP00000340684.3:p.Ala272=
ENST00000338702.3:c.816G>A	ENSP00000340684.3:p.Ala272=
ENST00000542639.5:c.417G>A	ENSP00000440846.1:p.Ala139=
NM_000240.3:c.816G>A	NP_000231.1:p.Ala272=
NM_001270458.1:c.417G>A	NP_001257387.1:p.Ala139=
NM_000240.4:c.816G>A MANE Select	NP_000231.1:p.Ala272=
NM_001270458.2:c.417G>A	NP_001257387.1:p.Ala139=