Canonical Allele Identifier: CA2426670020
Gene: MAOA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43731601A= , CM000685.2:g.43731601A= GRCh38
NC_000023.10:g.43590848A= , CM000685.1:g.43590848A= GRCh37
NC_000023.9:g.43475792A= NCBI36
NG_008957.2:g.80441A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000542639.6:c.397-93A= ENSP00000440846.1:n.397-93A=
ENST00000686683.1:c.106-93A= ENSP00000509063.1:n.106-93A=
ENST00000686980.1:n.928-93A=
ENST00000688006.1:c.397-93A= ENSP00000510311.1:n.397-93A=
ENST00000688859.1:n.352-93A=
ENST00000689087.1:c.397-93A= ENSP00000508997.1:n.397-93A=
ENST00000693128.1:c.691-93A= ENSP00000508493.1:n.691-93A=
ENST00000338702.4:c.796-93A= MANE Select ENSP00000340684.3:n.796-93A=
ENST00000338702.3:c.796-93A= ENSP00000340684.3:n.796-93A=
ENST00000542639.5:c.397-93A= ENSP00000440846.1:n.397-93A=
NM_000240.3:c.796-93A= NP_000231.1:n.796-93A=
NM_001270458.1:c.397-93A= NP_001257387.1:n.397-93A=
NM_000240.4:c.796-93A= MANE Select NP_000231.1:n.796-93A=
NM_001270458.2:c.397-93A= NP_001257387.1:n.397-93A=