Canonical Allele Identifier: CA2426669457
Gene: MAOA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43731836C= , CM000685.2:g.43731836C= GRCh38
NC_000023.10:g.43591083C= , CM000685.1:g.43591083C= GRCh37
NC_000023.9:g.43476027C= NCBI36
NG_008957.2:g.80676C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000542639.6:c.539C= ENSP00000440846.1:p.Ala180=
ENST00000686683.1:c.248C= ENSP00000509063.1:p.Ala83=
ENST00000686980.1:n.1070C=
ENST00000688006.1:c.539C= ENSP00000510311.1:p.Ala180=
ENST00000688859.1:n.494C=
ENST00000689087.1:c.539C= ENSP00000508997.1:p.Ala180=
ENST00000693128.1:c.833C= ENSP00000508493.1:p.Ala278=
ENST00000338702.4:c.938C= MANE Select ENSP00000340684.3:p.Ala313=
ENST00000338702.3:c.938C= ENSP00000340684.3:p.Ala313=
ENST00000542639.5:c.539C= ENSP00000440846.1:p.Ala180=
NM_000240.3:c.938C= NP_000231.1:p.Ala313=
NM_001270458.1:c.539C= NP_001257387.1:p.Ala180=
NM_000240.4:c.938C= MANE Select NP_000231.1:p.Ala313=
NM_001270458.2:c.539C= NP_001257387.1:p.Ala180=