Canonical Allele Identifier: CA329466107

Gene: MAOA

Linked Data

• dbSNP Id: rs769121201
• gnomAD v4: X-43731859-C-G
• MyVariant Identifiers: chrX:g.43591106C>G (hg19) ; chrX:g.43731859C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43731859C>G , CM000685.2:g.43731859C>G	GRCh38
NC_000023.10:g.43591106C>G , CM000685.1:g.43591106C>G	GRCh37
NC_000023.9:g.43476050C>G	NCBI36
NG_008957.2:g.80699C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542639.6:c.556+6C>G	ENSP00000440846.1:n.556+6C>G
ENST00000686683.1:c.265+6C>G	ENSP00000509063.1:n.265+6C>G
ENST00000686980.1:n.1087+6C>G
ENST00000688006.1:c.556+6C>G	ENSP00000510311.1:n.556+6C>G
ENST00000688859.1:n.511+6C>G
ENST00000689087.1:c.556+6C>G	ENSP00000508997.1:n.556+6C>G
ENST00000693128.1:c.850+6C>G	ENSP00000508493.1:n.850+6C>G
ENST00000338702.4:c.955+6C>G MANE Select	ENSP00000340684.3:n.955+6C>G
ENST00000338702.3:c.955+6C>G	ENSP00000340684.3:n.955+6C>G
ENST00000542639.5:c.556+6C>G	ENSP00000440846.1:n.556+6C>G
NM_000240.3:c.955+6C>G	NP_000231.1:n.955+6C>G
NM_001270458.1:c.556+6C>G	NP_001257387.1:n.556+6C>G
NM_000240.4:c.955+6C>G MANE Select	NP_000231.1:n.955+6C>G
NM_001270458.2:c.556+6C>G	NP_001257387.1:n.556+6C>G