Canonical Allele Identifier: CA2426669450
Gene: MAOA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43731793C= , CM000685.2:g.43731793C= GRCh38
NC_000023.10:g.43591040C= , CM000685.1:g.43591040C= GRCh37
NC_000023.9:g.43475984C= NCBI36
NG_008957.2:g.80633C=

Transcript Alleles

HGVS Amino-acid change
ENST00000542639.6:c.496C= ENSP00000440846.1:p.Pro166=
ENST00000686683.1:c.205C= ENSP00000509063.1:p.Pro69=
ENST00000686980.1:n.1027C=
ENST00000688006.1:c.496C= ENSP00000510311.1:p.Pro166=
ENST00000688859.1:n.451C=
ENST00000689087.1:c.496C= ENSP00000508997.1:p.Pro166=
ENST00000693128.1:c.790C= ENSP00000508493.1:p.Pro264=
ENST00000338702.4:c.895C= MANE Select ENSP00000340684.3:p.Pro299=
ENST00000338702.3:c.895C= ENSP00000340684.3:p.Pro299=
ENST00000542639.5:c.496C= ENSP00000440846.1:p.Pro166=
NM_000240.3:c.895C= NP_000231.1:p.Pro299=
NM_001270458.1:c.496C= NP_001257387.1:p.Pro166=
NM_000240.4:c.895C= MANE Select NP_000231.1:p.Pro299=
NM_001270458.2:c.496C= NP_001257387.1:p.Pro166=