Canonical Allele Identifier: CA413008292

Gene: MAOA

Linked Data

• MyVariant Identifiers: chrX:g.43591086T>C (hg19) ; chrX:g.43731839T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43731839T>C , CM000685.2:g.43731839T>C	GRCh38
NC_000023.10:g.43591086T>C , CM000685.1:g.43591086T>C	GRCh37
NC_000023.9:g.43476030T>C	NCBI36
NG_008957.2:g.80679T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542639.6:c.542T>C	ENSP00000440846.1:p.Phe181Ser
ENST00000686683.1:c.251T>C	ENSP00000509063.1:p.Phe84Ser
ENST00000686980.1:n.1073T>C
ENST00000688006.1:c.542T>C	ENSP00000510311.1:p.Phe181Ser
ENST00000688859.1:n.497T>C
ENST00000689087.1:c.542T>C	ENSP00000508997.1:p.Phe181Ser
ENST00000693128.1:c.836T>C	ENSP00000508493.1:p.Phe279Ser
ENST00000338702.4:c.941T>C MANE Select	ENSP00000340684.3:p.Phe314Ser
ENST00000338702.3:c.941T>C	ENSP00000340684.3:p.Phe314Ser
ENST00000542639.5:c.542T>C	ENSP00000440846.1:p.Phe181Ser
NM_000240.3:c.941T>C	NP_000231.1:p.Phe314Ser
NM_001270458.1:c.542T>C	NP_001257387.1:p.Phe181Ser
NM_000240.4:c.941T>C MANE Select	NP_000231.1:p.Phe314Ser
NM_001270458.2:c.542T>C	NP_001257387.1:p.Phe181Ser