Canonical Allele Identifier: CA2693509033
Gene: MAOA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43731775del , CM000685.2:g.43731775del GRCh38
NC_000023.10:g.43591022del , CM000685.1:g.43591022del GRCh37
NC_000023.9:g.43475966del NCBI36
NG_008957.2:g.80615del

Transcript Alleles

HGVS Amino-acid Change
ENST00000542639.6:c.478del ENSP00000440846.1:p.Gln160SerfsTer2
ENST00000686683.1:c.187del ENSP00000509063.1:p.Gln63SerfsTer2
ENST00000686980.1:n.1009del
ENST00000688006.1:c.478del ENSP00000510311.1:p.Gln160SerfsTer2
ENST00000688859.1:n.433del
ENST00000689087.1:c.478del ENSP00000508997.1:p.Gln160SerfsTer2
ENST00000693128.1:c.772del ENSP00000508493.1:p.Gln258SerfsTer2
ENST00000338702.4:c.877del MANE Select ENSP00000340684.3:p.Gln293SerfsTer2
ENST00000338702.3:c.877del ENSP00000340684.3:p.Gln293SerfsTer2
ENST00000542639.5:c.478del ENSP00000440846.1:p.Gln160SerfsTer2
NM_000240.3:c.877del NP_000231.1:p.Gln293SerfsTer2
NM_001270458.1:c.478del NP_001257387.1:p.Gln160SerfsTer2
NM_000240.4:c.877del MANE Select NP_000231.1:p.Gln293SerfsTer2
NM_001270458.2:c.478del NP_001257387.1:p.Gln160SerfsTer2