Canonical Allele Identifier: CA2580100941
Gene: MAOA HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43744182T>C , CM000685.2:g.43744182T>C GRCh38
NC_000023.10:g.43603429T>C , CM000685.1:g.43603429T>C GRCh37
NC_000023.9:g.43488373T>C NCBI36
NG_008957.2:g.93022T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000542639.6:c.1038+11T>C ENSP00000440846.1:n.1038+11T>C
ENST00000686683.1:c.747+11T>C ENSP00000509063.1:n.747+11T>C
ENST00000686980.1:n.5969+11T>C
ENST00000688006.1:c.1038+11T>C ENSP00000510311.1:n.1038+11T>C
ENST00000688859.1:n.993+11T>C
ENST00000689087.1:c.1038+11T>C ENSP00000508997.1:n.1038+11T>C
ENST00000693128.1:c.1332+11T>C ENSP00000508493.1:n.1332+11T>C
ENST00000338702.4:c.1437+11T>C MANE Select ENSP00000340684.3:n.1437+11T>C
ENST00000338702.3:c.1437+11T>C ENSP00000340684.3:n.1437+11T>C
ENST00000490604.1:n.265+11T>C
ENST00000542639.5:c.1038+11T>C ENSP00000440846.1:n.1038+11T>C
NM_000240.3:c.1437+11T>C NP_000231.1:n.1437+11T>C
NM_001270458.1:c.1038+11T>C NP_001257387.1:n.1038+11T>C
NM_000240.4:c.1437+11T>C MANE Select NP_000231.1:n.1437+11T>C
NM_001270458.2:c.1038+11T>C NP_001257387.1:n.1038+11T>C