Canonical Allele Identifier: CA413010788

Gene: MAOA

Linked Data

• gnomAD v4: X-43744369-C-G
• MyVariant Identifiers: chrX:g.43603616C>G (hg19) ; chrX:g.43744369C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43744369C>G , CM000685.2:g.43744369C>G	GRCh38
NC_000023.10:g.43603616C>G , CM000685.1:g.43603616C>G	GRCh37
NC_000023.9:g.43488560C>G	NCBI36
NG_008957.2:g.93209C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542639.6:c.1041C>G	ENSP00000440846.1:p.Asp347Glu
ENST00000686683.1:c.750C>G	ENSP00000509063.1:p.Asp250Glu
ENST00000686980.1:n.5972C>G
ENST00000688006.1:c.1041C>G	ENSP00000510311.1:p.Asp347Glu
ENST00000688859.1:n.996C>G
ENST00000689087.1:c.1041C>G	ENSP00000508997.1:p.Asp347Glu
ENST00000693128.1:c.1335C>G	ENSP00000508493.1:p.Asp445Glu
ENST00000338702.4:c.1440C>G MANE Select	ENSP00000340684.3:p.Asp480Glu
ENST00000338702.3:c.1440C>G	ENSP00000340684.3:p.Asp480Glu
ENST00000490604.1:n.268C>G
ENST00000542639.5:c.1041C>G	ENSP00000440846.1:p.Asp347Glu
NM_000240.3:c.1440C>G	NP_000231.1:p.Asp480Glu
NM_001270458.1:c.1041C>G	NP_001257387.1:p.Asp347Glu
NM_000240.4:c.1440C>G MANE Select	NP_000231.1:p.Asp480Glu
NM_001270458.2:c.1041C>G	NP_001257387.1:p.Asp347Glu