Canonical Allele Identifier: CA413007637

Gene: MAOA

Linked Data

• MyVariant Identifiers: chrX:g.43590992T>G (hg19) ; chrX:g.43731745T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43731745T>G , CM000685.2:g.43731745T>G	GRCh38
NC_000023.10:g.43590992T>G , CM000685.1:g.43590992T>G	GRCh37
NC_000023.9:g.43475936T>G	NCBI36
NG_008957.2:g.80585T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542639.6:c.448T>G	ENSP00000440846.1:p.Phe150Val
ENST00000686683.1:c.157T>G	ENSP00000509063.1:p.Phe53Val
ENST00000686980.1:n.979T>G
ENST00000688006.1:c.448T>G	ENSP00000510311.1:p.Phe150Val
ENST00000688859.1:n.403T>G
ENST00000689087.1:c.448T>G	ENSP00000508997.1:p.Phe150Val
ENST00000693128.1:c.742T>G	ENSP00000508493.1:p.Phe248Val
ENST00000338702.4:c.847T>G MANE Select	ENSP00000340684.3:p.Phe283Val
ENST00000338702.3:c.847T>G	ENSP00000340684.3:p.Phe283Val
ENST00000542639.5:c.448T>G	ENSP00000440846.1:p.Phe150Val
NM_000240.3:c.847T>G	NP_000231.1:p.Phe283Val
NM_001270458.1:c.448T>G	NP_001257387.1:p.Phe150Val
NM_000240.4:c.847T>G MANE Select	NP_000231.1:p.Phe283Val
NM_001270458.2:c.448T>G	NP_001257387.1:p.Phe150Val