Canonical Allele Identifier: CA2426670056
Gene: MAOA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43731722C= , CM000685.2:g.43731722C= GRCh38
NC_000023.10:g.43590969C= , CM000685.1:g.43590969C= GRCh37
NC_000023.9:g.43475913C= NCBI36
NG_008957.2:g.80562C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000542639.6:c.425C= ENSP00000440846.1:p.Pro142=
ENST00000686683.1:c.134C= ENSP00000509063.1:p.Pro45=
ENST00000686980.1:n.956C=
ENST00000688006.1:c.425C= ENSP00000510311.1:p.Pro142=
ENST00000688859.1:n.380C=
ENST00000689087.1:c.425C= ENSP00000508997.1:p.Pro142=
ENST00000693128.1:c.719C= ENSP00000508493.1:p.Pro240=
ENST00000338702.4:c.824C= MANE Select ENSP00000340684.3:p.Pro275=
ENST00000338702.3:c.824C= ENSP00000340684.3:p.Pro275=
ENST00000542639.5:c.425C= ENSP00000440846.1:p.Pro142=
NM_000240.3:c.824C= NP_000231.1:p.Pro275=
NM_001270458.1:c.425C= NP_001257387.1:p.Pro142=
NM_000240.4:c.824C= MANE Select NP_000231.1:p.Pro275=
NM_001270458.2:c.425C= NP_001257387.1:p.Pro142=