Canonical Allele Identifier: CA2426670009
Gene: MAOA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43731564T= , CM000685.2:g.43731564T= GRCh38
NC_000023.10:g.43590811T= , CM000685.1:g.43590811T= GRCh37
NC_000023.9:g.43475755T= NCBI36
NG_008957.2:g.80404T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000542639.6:c.397-130T= ENSP00000440846.1:n.397-130T=
ENST00000686683.1:c.106-130T= ENSP00000509063.1:n.106-130T=
ENST00000686980.1:n.928-130T=
ENST00000688006.1:c.397-130T= ENSP00000510311.1:n.397-130T=
ENST00000688859.1:n.352-130T=
ENST00000689087.1:c.397-130T= ENSP00000508997.1:n.397-130T=
ENST00000693128.1:c.691-130T= ENSP00000508493.1:n.691-130T=
ENST00000338702.4:c.796-130T= MANE Select ENSP00000340684.3:n.796-130T=
ENST00000338702.3:c.796-130T= ENSP00000340684.3:n.796-130T=
ENST00000542639.5:c.397-130T= ENSP00000440846.1:n.397-130T=
NM_000240.3:c.796-130T= NP_000231.1:n.796-130T=
NM_001270458.1:c.397-130T= NP_001257387.1:n.397-130T=
NM_000240.4:c.796-130T= MANE Select NP_000231.1:n.796-130T=
NM_001270458.2:c.397-130T= NP_001257387.1:n.397-130T=