Canonical Allele Identifier: CA329466106

Gene: MAOA

Linked Data

• dbSNP Id: rs1799835
• MyVariant Identifiers: chrX:g.43591085T>G (hg19) ; chrX:g.43731838T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43731838T>G , CM000685.2:g.43731838T>G	GRCh38
NC_000023.10:g.43591085T>G , CM000685.1:g.43591085T>G	GRCh37
NC_000023.9:g.43476029T>G	NCBI36
NG_008957.2:g.80678T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542639.6:c.541T>G	ENSP00000440846.1:p.Phe181Val
ENST00000686683.1:c.250T>G	ENSP00000509063.1:p.Phe84Val
ENST00000686980.1:n.1072T>G
ENST00000688006.1:c.541T>G	ENSP00000510311.1:p.Phe181Val
ENST00000688859.1:n.496T>G
ENST00000689087.1:c.541T>G	ENSP00000508997.1:p.Phe181Val
ENST00000693128.1:c.835T>G	ENSP00000508493.1:p.Phe279Val
ENST00000338702.4:c.940T>G MANE Select	ENSP00000340684.3:p.Phe314Val
ENST00000338702.3:c.940T>G	ENSP00000340684.3:p.Phe314Val
ENST00000542639.5:c.541T>G	ENSP00000440846.1:p.Phe181Val
NM_000240.3:c.940T>G	NP_000231.1:p.Phe314Val
NM_001270458.1:c.541T>G	NP_001257387.1:p.Phe181Val
NM_000240.4:c.940T>G MANE Select	NP_000231.1:p.Phe314Val
NM_001270458.2:c.541T>G	NP_001257387.1:p.Phe181Val