Canonical Allele Identifier: CA413008187

Gene: MAOA

Linked Data

• gnomAD v4: X-43731815-G-C
• MyVariant Identifiers: chrX:g.43591062G>C (hg19) ; chrX:g.43731815G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43731815G>C , CM000685.2:g.43731815G>C	GRCh38
NC_000023.10:g.43591062G>C , CM000685.1:g.43591062G>C	GRCh37
NC_000023.9:g.43476006G>C	NCBI36
NG_008957.2:g.80655G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542639.6:c.518G>C	ENSP00000440846.1:p.Cys173Ser
ENST00000686683.1:c.227G>C	ENSP00000509063.1:p.Cys76Ser
ENST00000686980.1:n.1049G>C
ENST00000688006.1:c.518G>C	ENSP00000510311.1:p.Cys173Ser
ENST00000688859.1:n.473G>C
ENST00000689087.1:c.518G>C	ENSP00000508997.1:p.Cys173Ser
ENST00000693128.1:c.812G>C	ENSP00000508493.1:p.Cys271Ser
ENST00000338702.4:c.917G>C MANE Select	ENSP00000340684.3:p.Cys306Ser
ENST00000338702.3:c.917G>C	ENSP00000340684.3:p.Cys306Ser
ENST00000542639.5:c.518G>C	ENSP00000440846.1:p.Cys173Ser
NM_000240.3:c.917G>C	NP_000231.1:p.Cys306Ser
NM_001270458.1:c.518G>C	NP_001257387.1:p.Cys173Ser
NM_000240.4:c.917G>C MANE Select	NP_000231.1:p.Cys306Ser
NM_001270458.2:c.518G>C	NP_001257387.1:p.Cys173Ser