Canonical Allele Identifier: CA2520378074
Gene: MAOA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43693932A>T , CM000685.2:g.43693932A>T GRCh38
NC_000023.10:g.43553179A>T , CM000685.1:g.43553179A>T GRCh37
NC_000023.9:g.43438123A>T NCBI36
NG_008957.2:g.42772A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000497485.2:n.942A>T
ENST00000542639.6:c.-94+504A>T ENSP00000440846.1:n.-94+504A>T
ENST00000686683.1:c.-305+504A>T ENSP00000509063.1:n.-305+504A>T
ENST00000686980.1:n.438+504A>T
ENST00000688006.1:c.-94+504A>T ENSP00000510311.1:n.-94+504A>T
ENST00000689087.1:c.-94+504A>T ENSP00000508997.1:n.-94+504A>T
ENST00000693128.1:c.306+504A>T ENSP00000508493.1:n.306+504A>T
ENST00000338702.4:c.306+504A>T MANE Select ENSP00000340684.3:n.306+504A>T
ENST00000338702.3:c.306+504A>T ENSP00000340684.3:n.306+504A>T
ENST00000497485.1:n.454+504A>T
ENST00000542639.5:c.-94+504A>T ENSP00000440846.1:n.-94+504A>T
NM_000240.3:c.306+504A>T NP_000231.1:n.306+504A>T
NM_001270458.1:c.-94+504A>T NP_001257387.1:n.-94+504A>T
NM_000240.4:c.306+504A>T MANE Select NP_000231.1:n.306+504A>T
NM_001270458.2:c.-94+504A>T NP_001257387.1:n.-94+504A>T