Canonical Allele Identifier: CA2426670055
Gene: MAOA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43731719C= , CM000685.2:g.43731719C= GRCh38
NC_000023.10:g.43590966C= , CM000685.1:g.43590966C= GRCh37
NC_000023.9:g.43475910C= NCBI36
NG_008957.2:g.80559C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000542639.6:c.422C= ENSP00000440846.1:p.Pro141=
ENST00000686683.1:c.131C= ENSP00000509063.1:p.Pro44=
ENST00000686980.1:n.953C=
ENST00000688006.1:c.422C= ENSP00000510311.1:p.Pro141=
ENST00000688859.1:n.377C=
ENST00000689087.1:c.422C= ENSP00000508997.1:p.Pro141=
ENST00000693128.1:c.716C= ENSP00000508493.1:p.Pro239=
ENST00000338702.4:c.821C= MANE Select ENSP00000340684.3:p.Pro274=
ENST00000338702.3:c.821C= ENSP00000340684.3:p.Pro274=
ENST00000542639.5:c.422C= ENSP00000440846.1:p.Pro141=
NM_000240.3:c.821C= NP_000231.1:p.Pro274=
NM_001270458.1:c.422C= NP_001257387.1:p.Pro141=
NM_000240.4:c.821C= MANE Select NP_000231.1:p.Pro274=
NM_001270458.2:c.422C= NP_001257387.1:p.Pro141=