Canonical Allele Identifier: CA2426670058
Gene: MAOA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43731728T= , CM000685.2:g.43731728T= GRCh38
NC_000023.10:g.43590975T= , CM000685.1:g.43590975T= GRCh37
NC_000023.9:g.43475919T= NCBI36
NG_008957.2:g.80568T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000542639.6:c.431T= ENSP00000440846.1:p.Leu144=
ENST00000686683.1:c.140T= ENSP00000509063.1:p.Leu47=
ENST00000686980.1:n.962T=
ENST00000688006.1:c.431T= ENSP00000510311.1:p.Leu144=
ENST00000688859.1:n.386T=
ENST00000689087.1:c.431T= ENSP00000508997.1:p.Leu144=
ENST00000693128.1:c.725T= ENSP00000508493.1:p.Leu242=
ENST00000338702.4:c.830T= MANE Select ENSP00000340684.3:p.Leu277=
ENST00000338702.3:c.830T= ENSP00000340684.3:p.Leu277=
ENST00000542639.5:c.431T= ENSP00000440846.1:p.Leu144=
NM_000240.3:c.830T= NP_000231.1:p.Leu277=
NM_001270458.1:c.431T= NP_001257387.1:p.Leu144=
NM_000240.4:c.830T= MANE Select NP_000231.1:p.Leu277=
NM_001270458.2:c.431T= NP_001257387.1:p.Leu144=