Canonical Allele Identifier: CA413008240

Gene: MAOA

Linked Data

• MyVariant Identifiers: chrX:g.43591070T>A (hg19) ; chrX:g.43731823T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43731823T>A , CM000685.2:g.43731823T>A	GRCh38
NC_000023.10:g.43591070T>A , CM000685.1:g.43591070T>A	GRCh37
NC_000023.9:g.43476014T>A	NCBI36
NG_008957.2:g.80663T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542639.6:c.526T>A	ENSP00000440846.1:p.Tyr176Asn
ENST00000686683.1:c.235T>A	ENSP00000509063.1:p.Tyr79Asn
ENST00000686980.1:n.1057T>A
ENST00000688006.1:c.526T>A	ENSP00000510311.1:p.Tyr176Asn
ENST00000688859.1:n.481T>A
ENST00000689087.1:c.526T>A	ENSP00000508997.1:p.Tyr176Asn
ENST00000693128.1:c.820T>A	ENSP00000508493.1:p.Tyr274Asn
ENST00000338702.4:c.925T>A MANE Select	ENSP00000340684.3:p.Tyr309Asn
ENST00000338702.3:c.925T>A	ENSP00000340684.3:p.Tyr309Asn
ENST00000542639.5:c.526T>A	ENSP00000440846.1:p.Tyr176Asn
NM_000240.3:c.925T>A	NP_000231.1:p.Tyr309Asn
NM_001270458.1:c.526T>A	NP_001257387.1:p.Tyr176Asn
NM_000240.4:c.925T>A MANE Select	NP_000231.1:p.Tyr309Asn
NM_001270458.2:c.526T>A	NP_001257387.1:p.Tyr176Asn