Canonical Allele Identifier: CA413004727

Gene: MAOA

Linked Data

• ClinVar Variation Id: 1418704
• ClinVar RCV Id: RCV001952245
• dbSNP Id: rs2147085459
• MyVariant Identifiers: chrX:g.43552659T>C (hg19) ; chrX:g.43693412T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43693412T>C , CM000685.2:g.43693412T>C	GRCh38
NC_000023.10:g.43552659T>C , CM000685.1:g.43552659T>C	GRCh37
NC_000023.9:g.43437603T>C	NCBI36
NG_008957.2:g.42252T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000497485.2:n.422T>C
ENST00000542639.6:c.-110T>C	ENSP00000440846.1:n.-110T>C
ENST00000686683.1:c.-321T>C	ENSP00000509063.1:n.-321T>C
ENST00000686980.1:n.422T>C
ENST00000688006.1:c.-110T>C	ENSP00000510311.1:n.-110T>C
ENST00000689087.1:c.-110T>C	ENSP00000508997.1:n.-110T>C
ENST00000693128.1:c.290T>C	ENSP00000508493.1:p.Leu97Pro
ENST00000338702.4:c.290T>C MANE Select	ENSP00000340684.3:p.Leu97Pro
ENST00000338702.3:c.290T>C	ENSP00000340684.3:p.Leu97Pro
ENST00000497485.1:n.438T>C
ENST00000542639.5:c.-110T>C	ENSP00000440846.1:n.-110T>C
NM_000240.3:c.290T>C	NP_000231.1:p.Leu97Pro
NM_001270458.1:c.-110T>C	NP_001257387.1:n.-110T>C
NM_000240.4:c.290T>C MANE Select	NP_000231.1:p.Leu97Pro
NM_001270458.2:c.-110T>C	NP_001257387.1:n.-110T>C