Canonical Allele Identifier: CA413007874

Gene: MAOA

Linked Data

• dbSNP Id: rs1469534616
• gnomAD v2: X-43591020-A-G
• MyVariant Identifiers: chrX:g.43591020A>G (hg19) ; chrX:g.43731773A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43731773A>G , CM000685.2:g.43731773A>G	GRCh38
NC_000023.10:g.43591020A>G , CM000685.1:g.43591020A>G	GRCh37
NC_000023.9:g.43475964A>G	NCBI36
NG_008957.2:g.80613A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542639.6:c.476A>G	ENSP00000440846.1:p.Asn159Ser
ENST00000686683.1:c.185A>G	ENSP00000509063.1:p.Asn62Ser
ENST00000686980.1:n.1007A>G
ENST00000688006.1:c.476A>G	ENSP00000510311.1:p.Asn159Ser
ENST00000688859.1:n.431A>G
ENST00000689087.1:c.476A>G	ENSP00000508997.1:p.Asn159Ser
ENST00000693128.1:c.770A>G	ENSP00000508493.1:p.Asn257Ser
ENST00000338702.4:c.875A>G MANE Select	ENSP00000340684.3:p.Asn292Ser
ENST00000338702.3:c.875A>G	ENSP00000340684.3:p.Asn292Ser
ENST00000542639.5:c.476A>G	ENSP00000440846.1:p.Asn159Ser
NM_000240.3:c.875A>G	NP_000231.1:p.Asn292Ser
NM_001270458.1:c.476A>G	NP_001257387.1:p.Asn159Ser
NM_000240.4:c.875A>G MANE Select	NP_000231.1:p.Asn292Ser
NM_001270458.2:c.476A>G	NP_001257387.1:p.Asn159Ser