Canonical Allele Identifier: CA413008121
Gene: MAOA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43731800G>T , CM000685.2:g.43731800G>T GRCh38
NC_000023.10:g.43591047G>T , CM000685.1:g.43591047G>T GRCh37
NC_000023.9:g.43475991G>T NCBI36
NG_008957.2:g.80640G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000542639.6:c.503G>T ENSP00000440846.1:p.Gly168Val
ENST00000686683.1:c.212G>T ENSP00000509063.1:p.Gly71Val
ENST00000686980.1:n.1034G>T
ENST00000688006.1:c.503G>T ENSP00000510311.1:p.Gly168Val
ENST00000688859.1:n.458G>T
ENST00000689087.1:c.503G>T ENSP00000508997.1:p.Gly168Val
ENST00000693128.1:c.797G>T ENSP00000508493.1:p.Gly266Val
ENST00000338702.4:c.902G>T MANE Select ENSP00000340684.3:p.Gly301Val
ENST00000338702.3:c.902G>T ENSP00000340684.3:p.Gly301Val
ENST00000542639.5:c.503G>T ENSP00000440846.1:p.Gly168Val
NM_000240.3:c.902G>T NP_000231.1:p.Gly301Val
NM_001270458.1:c.503G>T NP_001257387.1:p.Gly168Val
NM_000240.4:c.902G>T MANE Select NP_000231.1:p.Gly301Val
NM_001270458.2:c.503G>T NP_001257387.1:p.Gly168Val