Canonical Allele Identifier: CA2426669445
Gene: MAOA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43731784C= , CM000685.2:g.43731784C= GRCh38
NC_000023.10:g.43591031C= , CM000685.1:g.43591031C= GRCh37
NC_000023.9:g.43475975C= NCBI36
NG_008957.2:g.80624C=

Transcript Alleles

HGVS Amino-acid change
ENST00000542639.6:c.487C= ENSP00000440846.1:p.Gln163=
ENST00000686683.1:c.196C= ENSP00000509063.1:p.Gln66=
ENST00000686980.1:n.1018C=
ENST00000688006.1:c.487C= ENSP00000510311.1:p.Gln163=
ENST00000688859.1:n.442C=
ENST00000689087.1:c.487C= ENSP00000508997.1:p.Gln163=
ENST00000693128.1:c.781C= ENSP00000508493.1:p.Gln261=
ENST00000338702.4:c.886C= MANE Select ENSP00000340684.3:p.Gln296=
ENST00000338702.3:c.886C= ENSP00000340684.3:p.Gln296=
ENST00000542639.5:c.487C= ENSP00000440846.1:p.Gln163=
NM_000240.3:c.886C= NP_000231.1:p.Gln296=
NM_001270458.1:c.487C= NP_001257387.1:p.Gln163=
NM_000240.4:c.886C= MANE Select NP_000231.1:p.Gln296=
NM_001270458.2:c.487C= NP_001257387.1:p.Gln163=