Canonical Allele Identifier: CA516138135

Gene: MAOA

Linked Data

• MyVariant Identifiers: chrX:g.43591033G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43731786G>A , CM000685.2:g.43731786G>A	GRCh38
NC_000023.10:g.43591033G>A , CM000685.1:g.43591033G>A	GRCh37
NC_000023.9:g.43475977G>A	NCBI36
NG_008957.2:g.80626G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000542639.6:c.489G>A	ENSP00000440846.1:p.Gln163=
ENST00000686683.1:c.198G>A	ENSP00000509063.1:p.Gln66=
ENST00000686980.1:n.1020G>A
ENST00000688006.1:c.489G>A	ENSP00000510311.1:p.Gln163=
ENST00000688859.1:n.444G>A
ENST00000689087.1:c.489G>A	ENSP00000508997.1:p.Gln163=
ENST00000693128.1:c.783G>A	ENSP00000508493.1:p.Gln261=
ENST00000338702.4:c.888G>A MANE Select	ENSP00000340684.3:p.Gln296=
ENST00000338702.3:c.888G>A	ENSP00000340684.3:p.Gln296=
ENST00000542639.5:c.489G>A	ENSP00000440846.1:p.Gln163=
NM_000240.3:c.888G>A	NP_000231.1:p.Gln296=
NM_001270458.1:c.489G>A	NP_001257387.1:p.Gln163=
NM_000240.4:c.888G>A MANE Select	NP_000231.1:p.Gln296=
NM_001270458.2:c.489G>A	NP_001257387.1:p.Gln163=