Canonical Allele Identifier: CA2426669448
Gene: MAOA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43731789G= , CM000685.2:g.43731789G= GRCh38
NC_000023.10:g.43591036G= , CM000685.1:g.43591036G= GRCh37
NC_000023.9:g.43475980G= NCBI36
NG_008957.2:g.80629G=

Transcript Alleles

HGVS Amino-acid change
ENST00000542639.6:c.492G= ENSP00000440846.1:p.Arg164=
ENST00000686683.1:c.201G= ENSP00000509063.1:p.Arg67=
ENST00000686980.1:n.1023G=
ENST00000688006.1:c.492G= ENSP00000510311.1:p.Arg164=
ENST00000688859.1:n.447G=
ENST00000689087.1:c.492G= ENSP00000508997.1:p.Arg164=
ENST00000693128.1:c.786G= ENSP00000508493.1:p.Arg262=
ENST00000338702.4:c.891G= MANE Select ENSP00000340684.3:p.Arg297=
ENST00000338702.3:c.891G= ENSP00000340684.3:p.Arg297=
ENST00000542639.5:c.492G= ENSP00000440846.1:p.Arg164=
NM_000240.3:c.891G= NP_000231.1:p.Arg297=
NM_001270458.1:c.492G= NP_001257387.1:p.Arg164=
NM_000240.4:c.891G= MANE Select NP_000231.1:p.Arg297=
NM_001270458.2:c.492G= NP_001257387.1:p.Arg164=