Canonical Allele Identifier: CA2693509008

Gene: MAOA

Linked Data

• gnomAD v4: X-43731602-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43731602T>A , CM000685.2:g.43731602T>A	GRCh38
NC_000023.10:g.43590849T>A , CM000685.1:g.43590849T>A	GRCh37
NC_000023.9:g.43475793T>A	NCBI36
NG_008957.2:g.80442T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542639.6:c.397-92T>A	ENSP00000440846.1:n.397-92T>A
ENST00000686683.1:c.106-92T>A	ENSP00000509063.1:n.106-92T>A
ENST00000686980.1:n.928-92T>A
ENST00000688006.1:c.397-92T>A	ENSP00000510311.1:n.397-92T>A
ENST00000688859.1:n.352-92T>A
ENST00000689087.1:c.397-92T>A	ENSP00000508997.1:n.397-92T>A
ENST00000693128.1:c.691-92T>A	ENSP00000508493.1:n.691-92T>A
ENST00000338702.4:c.796-92T>A MANE Select	ENSP00000340684.3:n.796-92T>A
ENST00000338702.3:c.796-92T>A	ENSP00000340684.3:n.796-92T>A
ENST00000542639.5:c.397-92T>A	ENSP00000440846.1:n.397-92T>A
NM_000240.3:c.796-92T>A	NP_000231.1:n.796-92T>A
NM_001270458.1:c.397-92T>A	NP_001257387.1:n.397-92T>A
NM_000240.4:c.796-92T>A MANE Select	NP_000231.1:n.796-92T>A
NM_001270458.2:c.397-92T>A	NP_001257387.1:n.397-92T>A