Canonical Allele Identifier: CA2426673591
Gene: MAOA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43744144T= , CM000685.2:g.43744144T= GRCh38
NC_000023.10:g.43603391T= , CM000685.1:g.43603391T= GRCh37
NC_000023.9:g.43488335T= NCBI36
NG_008957.2:g.92984T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000542639.6:c.1011T= ENSP00000440846.1:p.Asp337=
ENST00000686683.1:c.720T= ENSP00000509063.1:p.Asp240=
ENST00000686980.1:n.5942T=
ENST00000688006.1:c.1011T= ENSP00000510311.1:p.Asp337=
ENST00000688859.1:n.966T=
ENST00000689087.1:c.1011T= ENSP00000508997.1:p.Asp337=
ENST00000693128.1:c.1305T= ENSP00000508493.1:p.Asp435=
ENST00000338702.4:c.1410T= MANE Select ENSP00000340684.3:p.Asp470=
ENST00000338702.3:c.1410T= ENSP00000340684.3:p.Asp470=
ENST00000490604.1:n.238T=
ENST00000542639.5:c.1011T= ENSP00000440846.1:p.Asp337=
NM_000240.3:c.1410T= NP_000231.1:p.Asp470=
NM_001270458.1:c.1011T= NP_001257387.1:p.Asp337=
NM_000240.4:c.1410T= MANE Select NP_000231.1:p.Asp470=
NM_001270458.2:c.1011T= NP_001257387.1:p.Asp337=