Canonical Allele Identifier: CA10390838

Gene: MAOA

Linked Data

• dbSNP Id: rs766232438
• ExAC: X:43590909 T / A
• gnomAD v2: X-43590909-T-A
• gnomAD v4: X-43731662-T-A
• MyVariant Identifiers: chrX:g.43590909T>A (hg19) ; chrX:g.43731662T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43731662T>A , CM000685.2:g.43731662T>A	GRCh38
NC_000023.10:g.43590909T>A , CM000685.1:g.43590909T>A	GRCh37
NC_000023.9:g.43475853T>A	NCBI36
NG_008957.2:g.80502T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542639.6:c.397-32T>A	ENSP00000440846.1:n.397-32T>A
ENST00000686683.1:c.106-32T>A	ENSP00000509063.1:n.106-32T>A
ENST00000686980.1:n.928-32T>A
ENST00000688006.1:c.397-32T>A	ENSP00000510311.1:n.397-32T>A
ENST00000688859.1:n.352-32T>A
ENST00000689087.1:c.397-32T>A	ENSP00000508997.1:n.397-32T>A
ENST00000693128.1:c.691-32T>A	ENSP00000508493.1:n.691-32T>A
ENST00000338702.4:c.796-32T>A MANE Select	ENSP00000340684.3:n.796-32T>A
ENST00000338702.3:c.796-32T>A	ENSP00000340684.3:n.796-32T>A
ENST00000542639.5:c.397-32T>A	ENSP00000440846.1:n.397-32T>A
NM_000240.3:c.796-32T>A	NP_000231.1:n.796-32T>A
NM_001270458.1:c.397-32T>A	NP_001257387.1:n.397-32T>A
NM_000240.4:c.796-32T>A MANE Select	NP_000231.1:n.796-32T>A
NM_001270458.2:c.397-32T>A	NP_001257387.1:n.397-32T>A