Canonical Allele Identifier: CA413007879

Gene: MAOA

Linked Data

• gnomAD v4: X-43731774-C-A
• MyVariant Identifiers: chrX:g.43591021C>A (hg19) ; chrX:g.43731774C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43731774C>A , CM000685.2:g.43731774C>A	GRCh38
NC_000023.10:g.43591021C>A , CM000685.1:g.43591021C>A	GRCh37
NC_000023.9:g.43475965C>A	NCBI36
NG_008957.2:g.80614C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542639.6:c.477C>A	ENSP00000440846.1:p.Asn159Lys
ENST00000686683.1:c.186C>A	ENSP00000509063.1:p.Asn62Lys
ENST00000686980.1:n.1008C>A
ENST00000688006.1:c.477C>A	ENSP00000510311.1:p.Asn159Lys
ENST00000688859.1:n.432C>A
ENST00000689087.1:c.477C>A	ENSP00000508997.1:p.Asn159Lys
ENST00000693128.1:c.771C>A	ENSP00000508493.1:p.Asn257Lys
ENST00000338702.4:c.876C>A MANE Select	ENSP00000340684.3:p.Asn292Lys
ENST00000338702.3:c.876C>A	ENSP00000340684.3:p.Asn292Lys
ENST00000542639.5:c.477C>A	ENSP00000440846.1:p.Asn159Lys
NM_000240.3:c.876C>A	NP_000231.1:p.Asn292Lys
NM_001270458.1:c.477C>A	NP_001257387.1:p.Asn159Lys
NM_000240.4:c.876C>A MANE Select	NP_000231.1:p.Asn292Lys
NM_001270458.2:c.477C>A	NP_001257387.1:p.Asn159Lys