Canonical Allele Identifier: CA516138133

Gene: MAOA

Linked Data

• MyVariant Identifiers: chrX:g.43591030T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43731783T>A , CM000685.2:g.43731783T>A	GRCh38
NC_000023.10:g.43591030T>A , CM000685.1:g.43591030T>A	GRCh37
NC_000023.9:g.43475974T>A	NCBI36
NG_008957.2:g.80623T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542639.6:c.486T>A	ENSP00000440846.1:p.Ile162=
ENST00000686683.1:c.195T>A	ENSP00000509063.1:p.Ile65=
ENST00000686980.1:n.1017T>A
ENST00000688006.1:c.486T>A	ENSP00000510311.1:p.Ile162=
ENST00000688859.1:n.441T>A
ENST00000689087.1:c.486T>A	ENSP00000508997.1:p.Ile162=
ENST00000693128.1:c.780T>A	ENSP00000508493.1:p.Ile260=
ENST00000338702.4:c.885T>A MANE Select	ENSP00000340684.3:p.Ile295=
ENST00000338702.3:c.885T>A	ENSP00000340684.3:p.Ile295=
ENST00000542639.5:c.486T>A	ENSP00000440846.1:p.Ile162=
NM_000240.3:c.885T>A	NP_000231.1:p.Ile295=
NM_001270458.1:c.486T>A	NP_001257387.1:p.Ile162=
NM_000240.4:c.885T>A MANE Select	NP_000231.1:p.Ile295=
NM_001270458.2:c.486T>A	NP_001257387.1:p.Ile162=