Canonical Allele Identifier: CA2426669458
Gene: MAOA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43731838T= , CM000685.2:g.43731838T= GRCh38
NC_000023.10:g.43591085T= , CM000685.1:g.43591085T= GRCh37
NC_000023.9:g.43476029T= NCBI36
NG_008957.2:g.80678T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000542639.6:c.541T= ENSP00000440846.1:p.Phe181=
ENST00000686683.1:c.250T= ENSP00000509063.1:p.Phe84=
ENST00000686980.1:n.1072T=
ENST00000688006.1:c.541T= ENSP00000510311.1:p.Phe181=
ENST00000688859.1:n.496T=
ENST00000689087.1:c.541T= ENSP00000508997.1:p.Phe181=
ENST00000693128.1:c.835T= ENSP00000508493.1:p.Phe279=
ENST00000338702.4:c.940T= MANE Select ENSP00000340684.3:p.Phe314=
ENST00000338702.3:c.940T= ENSP00000340684.3:p.Phe314=
ENST00000542639.5:c.541T= ENSP00000440846.1:p.Phe181=
NM_000240.3:c.940T= NP_000231.1:p.Phe314=
NM_001270458.1:c.541T= NP_001257387.1:p.Phe181=
NM_000240.4:c.940T= MANE Select NP_000231.1:p.Phe314=
NM_001270458.2:c.541T= NP_001257387.1:p.Phe181=