Canonical Allele Identifier: CA2426669451
Gene: MAOA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43731808A= , CM000685.2:g.43731808A= GRCh38
NC_000023.10:g.43591055A= , CM000685.1:g.43591055A= GRCh37
NC_000023.9:g.43475999A= NCBI36
NG_008957.2:g.80648A=

Transcript Alleles

HGVS Amino-acid change
ENST00000542639.6:c.511A= ENSP00000440846.1:p.Ile171=
ENST00000686683.1:c.220A= ENSP00000509063.1:p.Ile74=
ENST00000686980.1:n.1042A=
ENST00000688006.1:c.511A= ENSP00000510311.1:p.Ile171=
ENST00000688859.1:n.466A=
ENST00000689087.1:c.511A= ENSP00000508997.1:p.Ile171=
ENST00000693128.1:c.805A= ENSP00000508493.1:p.Ile269=
ENST00000338702.4:c.910A= MANE Select ENSP00000340684.3:p.Ile304=
ENST00000338702.3:c.910A= ENSP00000340684.3:p.Ile304=
ENST00000542639.5:c.511A= ENSP00000440846.1:p.Ile171=
NM_000240.3:c.910A= NP_000231.1:p.Ile304=
NM_001270458.1:c.511A= NP_001257387.1:p.Ile171=
NM_000240.4:c.910A= MANE Select NP_000231.1:p.Ile304=
NM_001270458.2:c.511A= NP_001257387.1:p.Ile171=