Canonical Allele Identifier: CA163205

Gene: MAOA

Linked Data

• ClinVar Variation Id: 139432
• ClinVar RCV Id: RCV000128399
• dbSNP Id: rs587777457
• MyVariant Identifiers: chrX:g.43590942G>T (hg19) ; chrX:g.43731695G>T (hg38)
• PubMed: PMID:24169519

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43731695G>T , CM000685.2:g.43731695G>T	GRCh38
NC_000023.10:g.43590942G>T , CM000685.1:g.43590942G>T	GRCh37
NC_000023.9:g.43475886G>T	NCBI36
NG_008957.2:g.80535G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000542639.6:c.398G>T	ENSP00000440846.1:p.Cys133Phe
ENST00000686683.1:c.107G>T	ENSP00000509063.1:p.Cys36Phe
ENST00000686980.1:n.929G>T
ENST00000688006.1:c.398G>T	ENSP00000510311.1:p.Cys133Phe
ENST00000688859.1:n.353G>T
ENST00000689087.1:c.398G>T	ENSP00000508997.1:p.Cys133Phe
ENST00000693128.1:c.692G>T	ENSP00000508493.1:p.Cys231Phe
ENST00000338702.4:c.797G>T MANE Select	ENSP00000340684.3:p.Cys266Phe
ENST00000338702.3:c.797G>T	ENSP00000340684.3:p.Cys266Phe
ENST00000542639.5:c.398G>T	ENSP00000440846.1:p.Cys133Phe
NM_000240.3:c.797G>T	NP_000231.1:p.Cys266Phe
NM_001270458.1:c.398G>T	NP_001257387.1:p.Cys133Phe
NM_000240.4:c.797G>T MANE Select	NP_000231.1:p.Cys266Phe
NM_001270458.2:c.398G>T	NP_001257387.1:p.Cys133Phe