Canonical Allele Identifier: CA413008074

Gene: MAOA

Linked Data

• COSMIC: COSM4950441
• MyVariant Identifiers: chrX:g.43591043A>G (hg19) ; chrX:g.43731796A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43731796A>G , CM000685.2:g.43731796A>G	GRCh38
NC_000023.10:g.43591043A>G , CM000685.1:g.43591043A>G	GRCh37
NC_000023.9:g.43475987A>G	NCBI36
NG_008957.2:g.80636A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000542639.6:c.499A>G	ENSP00000440846.1:p.Met167Val
ENST00000686683.1:c.208A>G	ENSP00000509063.1:p.Met70Val
ENST00000686980.1:n.1030A>G
ENST00000688006.1:c.499A>G	ENSP00000510311.1:p.Met167Val
ENST00000688859.1:n.454A>G
ENST00000689087.1:c.499A>G	ENSP00000508997.1:p.Met167Val
ENST00000693128.1:c.793A>G	ENSP00000508493.1:p.Met265Val
ENST00000338702.4:c.898A>G MANE Select	ENSP00000340684.3:p.Met300Val
ENST00000338702.3:c.898A>G	ENSP00000340684.3:p.Met300Val
ENST00000542639.5:c.499A>G	ENSP00000440846.1:p.Met167Val
NM_000240.3:c.898A>G	NP_000231.1:p.Met300Val
NM_001270458.1:c.499A>G	NP_001257387.1:p.Met167Val
NM_000240.4:c.898A>G MANE Select	NP_000231.1:p.Met300Val
NM_001270458.2:c.499A>G	NP_001257387.1:p.Met167Val