Canonical Allele Identifier: CA413007804

Gene: MAOA

Linked Data

• MyVariant Identifiers: chrX:g.43591013G>C (hg19) ; chrX:g.43731766G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43731766G>C , CM000685.2:g.43731766G>C	GRCh38
NC_000023.10:g.43591013G>C , CM000685.1:g.43591013G>C	GRCh37
NC_000023.9:g.43475957G>C	NCBI36
NG_008957.2:g.80606G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542639.6:c.469G>C	ENSP00000440846.1:p.Glu157Gln
ENST00000686683.1:c.178G>C	ENSP00000509063.1:p.Glu60Gln
ENST00000686980.1:n.1000G>C
ENST00000688006.1:c.469G>C	ENSP00000510311.1:p.Glu157Gln
ENST00000688859.1:n.424G>C
ENST00000689087.1:c.469G>C	ENSP00000508997.1:p.Glu157Gln
ENST00000693128.1:c.763G>C	ENSP00000508493.1:p.Glu255Gln
ENST00000338702.4:c.868G>C MANE Select	ENSP00000340684.3:p.Glu290Gln
ENST00000338702.3:c.868G>C	ENSP00000340684.3:p.Glu290Gln
ENST00000542639.5:c.469G>C	ENSP00000440846.1:p.Glu157Gln
NM_000240.3:c.868G>C	NP_000231.1:p.Glu290Gln
NM_001270458.1:c.469G>C	NP_001257387.1:p.Glu157Gln
NM_000240.4:c.868G>C MANE Select	NP_000231.1:p.Glu290Gln
NM_001270458.2:c.469G>C	NP_001257387.1:p.Glu157Gln