Canonical Allele Identifier: CA2820649444
Gene: MAOA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43731784del , CM000685.2:g.43731784del GRCh38
NC_000023.10:g.43591031del , CM000685.1:g.43591031del GRCh37
NC_000023.9:g.43475975del NCBI36
NG_008957.2:g.80624del

Transcript Alleles

HGVS Amino-acid Change
ENST00000542639.6:c.487del ENSP00000440846.1:p.Gln163SerfsTer12
ENST00000686683.1:c.196del ENSP00000509063.1:p.Gln66SerfsTer12
ENST00000686980.1:n.1018del
ENST00000688006.1:c.487del ENSP00000510311.1:p.Gln163SerfsTer12
ENST00000688859.1:n.442del
ENST00000689087.1:c.487del ENSP00000508997.1:p.Gln163SerfsTer12
ENST00000693128.1:c.781del ENSP00000508493.1:p.Gln261SerfsTer12
ENST00000338702.4:c.886del MANE Select ENSP00000340684.3:p.Gln296SerfsTer12
ENST00000338702.3:c.886del ENSP00000340684.3:p.Gln296SerfsTer12
ENST00000542639.5:c.487del ENSP00000440846.1:p.Gln163SerfsTer12
NM_000240.3:c.886del NP_000231.1:p.Gln296SerfsTer12
NM_001270458.1:c.487del NP_001257387.1:p.Gln163SerfsTer12
NM_000240.4:c.886del MANE Select NP_000231.1:p.Gln296SerfsTer12
NM_001270458.2:c.487del NP_001257387.1:p.Gln163SerfsTer12