Canonical Allele Identifier: CA2693509047

Gene: MAOA

Linked Data

• gnomAD v4: X-43731891-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43731891G>A , CM000685.2:g.43731891G>A	GRCh38
NC_000023.10:g.43591138G>A , CM000685.1:g.43591138G>A	GRCh37
NC_000023.9:g.43476082G>A	NCBI36
NG_008957.2:g.80731G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542639.6:c.556+38G>A	ENSP00000440846.1:n.556+38G>A
ENST00000686683.1:c.265+38G>A	ENSP00000509063.1:n.265+38G>A
ENST00000686980.1:n.1087+38G>A
ENST00000688006.1:c.556+38G>A	ENSP00000510311.1:n.556+38G>A
ENST00000688859.1:n.511+38G>A
ENST00000689087.1:c.556+38G>A	ENSP00000508997.1:n.556+38G>A
ENST00000693128.1:c.850+38G>A	ENSP00000508493.1:n.850+38G>A
ENST00000338702.4:c.955+38G>A MANE Select	ENSP00000340684.3:n.955+38G>A
ENST00000338702.3:c.955+38G>A	ENSP00000340684.3:n.955+38G>A
ENST00000542639.5:c.556+38G>A	ENSP00000440846.1:n.556+38G>A
NM_000240.3:c.955+38G>A	NP_000231.1:n.955+38G>A
NM_001270458.1:c.556+38G>A	NP_001257387.1:n.556+38G>A
NM_000240.4:c.955+38G>A MANE Select	NP_000231.1:n.955+38G>A
NM_001270458.2:c.556+38G>A	NP_001257387.1:n.556+38G>A