Canonical Allele Identifier: CA413008311

Gene: MAOA

Linked Data

• MyVariant Identifiers: chrX:g.43591089G>C (hg19) ; chrX:g.43731842G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43731842G>C , CM000685.2:g.43731842G>C	GRCh38
NC_000023.10:g.43591089G>C , CM000685.1:g.43591089G>C	GRCh37
NC_000023.9:g.43476033G>C	NCBI36
NG_008957.2:g.80682G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542639.6:c.545G>C	ENSP00000440846.1:p.Trp182Ser
ENST00000686683.1:c.254G>C	ENSP00000509063.1:p.Trp85Ser
ENST00000686980.1:n.1076G>C
ENST00000688006.1:c.545G>C	ENSP00000510311.1:p.Trp182Ser
ENST00000688859.1:n.500G>C
ENST00000689087.1:c.545G>C	ENSP00000508997.1:p.Trp182Ser
ENST00000693128.1:c.839G>C	ENSP00000508493.1:p.Trp280Ser
ENST00000338702.4:c.944G>C MANE Select	ENSP00000340684.3:p.Trp315Ser
ENST00000338702.3:c.944G>C	ENSP00000340684.3:p.Trp315Ser
ENST00000542639.5:c.545G>C	ENSP00000440846.1:p.Trp182Ser
NM_000240.3:c.944G>C	NP_000231.1:p.Trp315Ser
NM_001270458.1:c.545G>C	NP_001257387.1:p.Trp182Ser
NM_000240.4:c.944G>C MANE Select	NP_000231.1:p.Trp315Ser
NM_001270458.2:c.545G>C	NP_001257387.1:p.Trp182Ser