Canonical Allele Identifier: CA2693508991

Gene: MAOA

Linked Data

• gnomAD v4: X-43731575-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43731575C>T , CM000685.2:g.43731575C>T	GRCh38
NC_000023.10:g.43590822C>T , CM000685.1:g.43590822C>T	GRCh37
NC_000023.9:g.43475766C>T	NCBI36
NG_008957.2:g.80415C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542639.6:c.397-119C>T	ENSP00000440846.1:n.397-119C>T
ENST00000686683.1:c.106-119C>T	ENSP00000509063.1:n.106-119C>T
ENST00000686980.1:n.928-119C>T
ENST00000688006.1:c.397-119C>T	ENSP00000510311.1:n.397-119C>T
ENST00000688859.1:n.352-119C>T
ENST00000689087.1:c.397-119C>T	ENSP00000508997.1:n.397-119C>T
ENST00000693128.1:c.691-119C>T	ENSP00000508493.1:n.691-119C>T
ENST00000338702.4:c.796-119C>T MANE Select	ENSP00000340684.3:n.796-119C>T
ENST00000338702.3:c.796-119C>T	ENSP00000340684.3:n.796-119C>T
ENST00000542639.5:c.397-119C>T	ENSP00000440846.1:n.397-119C>T
NM_000240.3:c.796-119C>T	NP_000231.1:n.796-119C>T
NM_001270458.1:c.397-119C>T	NP_001257387.1:n.397-119C>T
NM_000240.4:c.796-119C>T MANE Select	NP_000231.1:n.796-119C>T
NM_001270458.2:c.397-119C>T	NP_001257387.1:n.397-119C>T