Canonical Allele Identifier: CA413008170
Gene: MAOA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43731812A>T , CM000685.2:g.43731812A>T GRCh38
NC_000023.10:g.43591059A>T , CM000685.1:g.43591059A>T GRCh37
NC_000023.9:g.43476003A>T NCBI36
NG_008957.2:g.80652A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000542639.6:c.515A>T ENSP00000440846.1:p.Lys172Met
ENST00000686683.1:c.224A>T ENSP00000509063.1:p.Lys75Met
ENST00000686980.1:n.1046A>T
ENST00000688006.1:c.515A>T ENSP00000510311.1:p.Lys172Met
ENST00000688859.1:n.470A>T
ENST00000689087.1:c.515A>T ENSP00000508997.1:p.Lys172Met
ENST00000693128.1:c.809A>T ENSP00000508493.1:p.Lys270Met
ENST00000338702.4:c.914A>T MANE Select ENSP00000340684.3:p.Lys305Met
ENST00000338702.3:c.914A>T ENSP00000340684.3:p.Lys305Met
ENST00000542639.5:c.515A>T ENSP00000440846.1:p.Lys172Met
NM_000240.3:c.914A>T NP_000231.1:p.Lys305Met
NM_001270458.1:c.515A>T NP_001257387.1:p.Lys172Met
NM_000240.4:c.914A>T MANE Select NP_000231.1:p.Lys305Met
NM_001270458.2:c.515A>T NP_001257387.1:p.Lys172Met