Canonical Allele Identifier: CA2426670050
Gene: MAOA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43731702C= , CM000685.2:g.43731702C= GRCh38
NC_000023.10:g.43590949C= , CM000685.1:g.43590949C= GRCh37
NC_000023.9:g.43475893C= NCBI36
NG_008957.2:g.80542C=

Transcript Alleles

HGVS Amino-acid change
ENST00000542639.6:c.405C= ENSP00000440846.1:p.Tyr135=
ENST00000686683.1:c.114C= ENSP00000509063.1:p.Tyr38=
ENST00000686980.1:n.936C=
ENST00000688006.1:c.405C= ENSP00000510311.1:p.Tyr135=
ENST00000688859.1:n.360C=
ENST00000689087.1:c.405C= ENSP00000508997.1:p.Tyr135=
ENST00000693128.1:c.699C= ENSP00000508493.1:p.Tyr233=
ENST00000338702.4:c.804C= MANE Select ENSP00000340684.3:p.Tyr268=
ENST00000338702.3:c.804C= ENSP00000340684.3:p.Tyr268=
ENST00000542639.5:c.405C= ENSP00000440846.1:p.Tyr135=
NM_000240.3:c.804C= NP_000231.1:p.Tyr268=
NM_001270458.1:c.405C= NP_001257387.1:p.Tyr135=
NM_000240.4:c.804C= MANE Select NP_000231.1:p.Tyr268=
NM_001270458.2:c.405C= NP_001257387.1:p.Tyr135=