Canonical Allele Identifier: CA413007798

Gene: MAOA

Linked Data

• MyVariant Identifiers: chrX:g.43591011C>G (hg19) ; chrX:g.43731764C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43731764C>G , CM000685.2:g.43731764C>G	GRCh38
NC_000023.10:g.43591011C>G , CM000685.1:g.43591011C>G	GRCh37
NC_000023.9:g.43475955C>G	NCBI36
NG_008957.2:g.80604C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542639.6:c.467C>G	ENSP00000440846.1:p.Ala156Gly
ENST00000686683.1:c.176C>G	ENSP00000509063.1:p.Ala59Gly
ENST00000686980.1:n.998C>G
ENST00000688006.1:c.467C>G	ENSP00000510311.1:p.Ala156Gly
ENST00000688859.1:n.422C>G
ENST00000689087.1:c.467C>G	ENSP00000508997.1:p.Ala156Gly
ENST00000693128.1:c.761C>G	ENSP00000508493.1:p.Ala254Gly
ENST00000338702.4:c.866C>G MANE Select	ENSP00000340684.3:p.Ala289Gly
ENST00000338702.3:c.866C>G	ENSP00000340684.3:p.Ala289Gly
ENST00000542639.5:c.467C>G	ENSP00000440846.1:p.Ala156Gly
NM_000240.3:c.866C>G	NP_000231.1:p.Ala289Gly
NM_001270458.1:c.467C>G	NP_001257387.1:p.Ala156Gly
NM_000240.4:c.866C>G MANE Select	NP_000231.1:p.Ala289Gly
NM_001270458.2:c.467C>G	NP_001257387.1:p.Ala156Gly