Canonical Allele Identifier: CA10390841

Gene: MAOA

Linked Data

• ClinVar Variation Id: 3024250
• ClinVar RCV Id: RCV003883296
• dbSNP Id: rs755014579
• ExAC: X:43590931 T / C
• gnomAD v2: X-43590931-T-C
• gnomAD v3: X-43731684-T-C
• gnomAD v4: X-43731684-T-C
• MyVariant Identifiers: chrX:g.43590931T>C (hg19) ; chrX:g.43731684T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43731684T>C , CM000685.2:g.43731684T>C	GRCh38
NC_000023.10:g.43590931T>C , CM000685.1:g.43590931T>C	GRCh37
NC_000023.9:g.43475875T>C	NCBI36
NG_008957.2:g.80524T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000542639.6:c.397-10T>C	ENSP00000440846.1:n.397-10T>C
ENST00000686683.1:c.106-10T>C	ENSP00000509063.1:n.106-10T>C
ENST00000686980.1:n.928-10T>C
ENST00000688006.1:c.397-10T>C	ENSP00000510311.1:n.397-10T>C
ENST00000688859.1:n.352-10T>C
ENST00000689087.1:c.397-10T>C	ENSP00000508997.1:n.397-10T>C
ENST00000693128.1:c.691-10T>C	ENSP00000508493.1:n.691-10T>C
ENST00000338702.4:c.796-10T>C MANE Select	ENSP00000340684.3:n.796-10T>C
ENST00000338702.3:c.796-10T>C	ENSP00000340684.3:n.796-10T>C
ENST00000542639.5:c.397-10T>C	ENSP00000440846.1:n.397-10T>C
NM_000240.3:c.796-10T>C	NP_000231.1:n.796-10T>C
NM_001270458.1:c.397-10T>C	NP_001257387.1:n.397-10T>C
NM_000240.4:c.796-10T>C MANE Select	NP_000231.1:n.796-10T>C
NM_001270458.2:c.397-10T>C	NP_001257387.1:n.397-10T>C