Canonical Allele Identifier: CA2426669459
Gene: MAOA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43731852G= , CM000685.2:g.43731852G= GRCh38
NC_000023.10:g.43591099G= , CM000685.1:g.43591099G= GRCh37
NC_000023.9:g.43476043G= NCBI36
NG_008957.2:g.80692G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000542639.6:c.555G= ENSP00000440846.1:p.Lys185=
ENST00000686683.1:c.264G= ENSP00000509063.1:p.Lys88=
ENST00000686980.1:n.1086G=
ENST00000688006.1:c.555G= ENSP00000510311.1:p.Lys185=
ENST00000688859.1:n.510G=
ENST00000689087.1:c.555G= ENSP00000508997.1:p.Lys185=
ENST00000693128.1:c.849G= ENSP00000508493.1:p.Lys283=
ENST00000338702.4:c.954G= MANE Select ENSP00000340684.3:p.Lys318=
ENST00000338702.3:c.954G= ENSP00000340684.3:p.Lys318=
ENST00000542639.5:c.555G= ENSP00000440846.1:p.Lys185=
NM_000240.3:c.954G= NP_000231.1:p.Lys318=
NM_001270458.1:c.555G= NP_001257387.1:p.Lys185=
NM_000240.4:c.954G= MANE Select NP_000231.1:p.Lys318=
NM_001270458.2:c.555G= NP_001257387.1:p.Lys185=