Canonical Allele Identifier: CA329466105

Gene: MAOA

Linked Data

• dbSNP Id: rs866082662
• MyVariant Identifiers: chrX:g.43591077A>G (hg19) ; chrX:g.43731830A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43731830A>G , CM000685.2:g.43731830A>G	GRCh38
NC_000023.10:g.43591077A>G , CM000685.1:g.43591077A>G	GRCh37
NC_000023.9:g.43476021A>G	NCBI36
NG_008957.2:g.80670A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542639.6:c.533A>G	ENSP00000440846.1:p.Lys178Arg
ENST00000686683.1:c.242A>G	ENSP00000509063.1:p.Lys81Arg
ENST00000686980.1:n.1064A>G
ENST00000688006.1:c.533A>G	ENSP00000510311.1:p.Lys178Arg
ENST00000688859.1:n.488A>G
ENST00000689087.1:c.533A>G	ENSP00000508997.1:p.Lys178Arg
ENST00000693128.1:c.827A>G	ENSP00000508493.1:p.Lys276Arg
ENST00000338702.4:c.932A>G MANE Select	ENSP00000340684.3:p.Lys311Arg
ENST00000338702.3:c.932A>G	ENSP00000340684.3:p.Lys311Arg
ENST00000542639.5:c.533A>G	ENSP00000440846.1:p.Lys178Arg
NM_000240.3:c.932A>G	NP_000231.1:p.Lys311Arg
NM_001270458.1:c.533A>G	NP_001257387.1:p.Lys178Arg
NM_000240.4:c.932A>G MANE Select	NP_000231.1:p.Lys311Arg
NM_001270458.2:c.533A>G	NP_001257387.1:p.Lys178Arg