Canonical Allele Identifier: CA875558345

Gene: MAOA

Linked Data

• dbSNP Id: rs746608642
• gnomAD v3: X-43740289-T-C
• gnomAD v4: X-43740289-T-C
• MyVariant Identifiers: chrX:g.43599536T>C (hg19) ; chrX:g.43740289T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43740289T>C , CM000685.2:g.43740289T>C	GRCh38
NC_000023.10:g.43599536T>C , CM000685.1:g.43599536T>C	GRCh37
NC_000023.9:g.43484480T>C	NCBI36
NG_008957.2:g.89129T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000542639.6:c.708-392T>C	ENSP00000440846.1:n.708-392T>C
ENST00000686683.1:c.417-392T>C	ENSP00000509063.1:n.417-392T>C
ENST00000686980.1:n.5247T>C
ENST00000688006.1:c.708-392T>C	ENSP00000510311.1:n.708-392T>C
ENST00000688859.1:n.663-392T>C
ENST00000689087.1:c.708-392T>C	ENSP00000508997.1:n.708-392T>C
ENST00000693128.1:c.1002-392T>C	ENSP00000508493.1:n.1002-392T>C
ENST00000338702.4:c.1107-392T>C MANE Select	ENSP00000340684.3:n.1107-392T>C
ENST00000338702.3:c.1107-392T>C	ENSP00000340684.3:n.1107-392T>C
ENST00000542639.5:c.708-392T>C	ENSP00000440846.1:n.708-392T>C
NM_000240.3:c.1107-392T>C	NP_000231.1:n.1107-392T>C
NM_001270458.1:c.708-392T>C	NP_001257387.1:n.708-392T>C
NM_000240.4:c.1107-392T>C MANE Select	NP_000231.1:n.1107-392T>C
NM_001270458.2:c.708-392T>C	NP_001257387.1:n.708-392T>C