Canonical Allele Identifier: CA329466102

Gene: MAOA

Linked Data

• ClinVar Variation Id: 1064570
• ClinVar RCV Id: RCV001374617
• dbSNP Id: rs150176511
• gnomAD v2: X-43590950-G-A
• gnomAD v3: X-43731703-G-A
• gnomAD v4: X-43731703-G-A
• COSMIC: COSM5515861
• MyVariant Identifiers: chrX:g.43590950G>A (hg19) ; chrX:g.43731703G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43731703G>A , CM000685.2:g.43731703G>A	GRCh38
NC_000023.10:g.43590950G>A , CM000685.1:g.43590950G>A	GRCh37
NC_000023.9:g.43475894G>A	NCBI36
NG_008957.2:g.80543G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000542639.6:c.406G>A	ENSP00000440846.1:p.Val136Ile
ENST00000686683.1:c.115G>A	ENSP00000509063.1:p.Val39Ile
ENST00000686980.1:n.937G>A
ENST00000688006.1:c.406G>A	ENSP00000510311.1:p.Val136Ile
ENST00000688859.1:n.361G>A
ENST00000689087.1:c.406G>A	ENSP00000508997.1:p.Val136Ile
ENST00000693128.1:c.700G>A	ENSP00000508493.1:p.Val234Ile
ENST00000338702.4:c.805G>A MANE Select	ENSP00000340684.3:p.Val269Ile
ENST00000338702.3:c.805G>A	ENSP00000340684.3:p.Val269Ile
ENST00000542639.5:c.406G>A	ENSP00000440846.1:p.Val136Ile
NM_000240.3:c.805G>A	NP_000231.1:p.Val269Ile
NM_001270458.1:c.406G>A	NP_001257387.1:p.Val136Ile
NM_000240.4:c.805G>A MANE Select	NP_000231.1:p.Val269Ile
NM_001270458.2:c.406G>A	NP_001257387.1:p.Val136Ile