Canonical Allele Identifier: CA2426657722

Gene: MAOA

Linked Data

• dbSNP Id: rs2033557980
• gnomAD v3: X-43693937-G-A
• gnomAD v4: X-43693937-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43693937G>A , CM000685.2:g.43693937G>A	GRCh38
NC_000023.10:g.43553184G>A , CM000685.1:g.43553184G>A	GRCh37
NC_000023.9:g.43438128G>A	NCBI36
NG_008957.2:g.42777G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000497485.2:n.947G>A
ENST00000542639.6:c.-94+509G>A	ENSP00000440846.1:n.-94+509G>A
ENST00000686683.1:c.-305+509G>A	ENSP00000509063.1:n.-305+509G>A
ENST00000686980.1:n.438+509G>A
ENST00000688006.1:c.-94+509G>A	ENSP00000510311.1:n.-94+509G>A
ENST00000689087.1:c.-94+509G>A	ENSP00000508997.1:n.-94+509G>A
ENST00000693128.1:c.306+509G>A	ENSP00000508493.1:n.306+509G>A
ENST00000338702.4:c.306+509G>A MANE Select	ENSP00000340684.3:n.306+509G>A
ENST00000338702.3:c.306+509G>A	ENSP00000340684.3:n.306+509G>A
ENST00000497485.1:n.454+509G>A
ENST00000542639.5:c.-94+509G>A	ENSP00000440846.1:n.-94+509G>A
NM_000240.3:c.306+509G>A	NP_000231.1:n.306+509G>A
NM_001270458.1:c.-94+509G>A	NP_001257387.1:n.-94+509G>A
NM_000240.4:c.306+509G>A MANE Select	NP_000231.1:n.306+509G>A
NM_001270458.2:c.-94+509G>A	NP_001257387.1:n.-94+509G>A