Canonical Allele Identifier: CA516138082

Gene: MAOA

Linked Data

• dbSNP Id: rs1251997167
• gnomAD v2: X-43590952-A-G
• gnomAD v3: X-43731705-A-G
• gnomAD v4: X-43731705-A-G
• MyVariant Identifiers: chrX:g.43590952A>G (hg19) ; chrX:g.43731705A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43731705A>G , CM000685.2:g.43731705A>G	GRCh38
NC_000023.10:g.43590952A>G , CM000685.1:g.43590952A>G	GRCh37
NC_000023.9:g.43475896A>G	NCBI36
NG_008957.2:g.80545A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000542639.6:c.408A>G	ENSP00000440846.1:p.Val136=
ENST00000686683.1:c.117A>G	ENSP00000509063.1:p.Val39=
ENST00000686980.1:n.939A>G
ENST00000688006.1:c.408A>G	ENSP00000510311.1:p.Val136=
ENST00000688859.1:n.363A>G
ENST00000689087.1:c.408A>G	ENSP00000508997.1:p.Val136=
ENST00000693128.1:c.702A>G	ENSP00000508493.1:p.Val234=
ENST00000338702.4:c.807A>G MANE Select	ENSP00000340684.3:p.Val269=
ENST00000338702.3:c.807A>G	ENSP00000340684.3:p.Val269=
ENST00000542639.5:c.408A>G	ENSP00000440846.1:p.Val136=
NM_000240.3:c.807A>G	NP_000231.1:p.Val269=
NM_001270458.1:c.408A>G	NP_001257387.1:p.Val136=
NM_000240.4:c.807A>G MANE Select	NP_000231.1:p.Val269=
NM_001270458.2:c.408A>G	NP_001257387.1:p.Val136=