Canonical Allele Identifier: CA2426669456
Gene: MAOA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43731831G= , CM000685.2:g.43731831G= GRCh38
NC_000023.10:g.43591078G= , CM000685.1:g.43591078G= GRCh37
NC_000023.9:g.43476022G= NCBI36
NG_008957.2:g.80671G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000542639.6:c.534G= ENSP00000440846.1:p.Lys178=
ENST00000686683.1:c.243G= ENSP00000509063.1:p.Lys81=
ENST00000686980.1:n.1065G=
ENST00000688006.1:c.534G= ENSP00000510311.1:p.Lys178=
ENST00000688859.1:n.489G=
ENST00000689087.1:c.534G= ENSP00000508997.1:p.Lys178=
ENST00000693128.1:c.828G= ENSP00000508493.1:p.Lys276=
ENST00000338702.4:c.933G= MANE Select ENSP00000340684.3:p.Lys311=
ENST00000338702.3:c.933G= ENSP00000340684.3:p.Lys311=
ENST00000542639.5:c.534G= ENSP00000440846.1:p.Lys178=
NM_000240.3:c.933G= NP_000231.1:p.Lys311=
NM_001270458.1:c.534G= NP_001257387.1:p.Lys178=
NM_000240.4:c.933G= MANE Select NP_000231.1:p.Lys311=
NM_001270458.2:c.534G= NP_001257387.1:p.Lys178=