Canonical Allele Identifier: CA10390859

Gene: MAOA

Linked Data

• dbSNP Id: rs113519998
• ExAC: X:43591145 TCA / T
• gnomAD v2: X-43591145-TCA-T
• gnomAD v3: X-43731898-TCA-T
• gnomAD v4: X-43731898-TCA-T
• MyVariant Identifiers: chrX:g.43591146_43591147del (hg19) ; chrX:g.43731899_43731900del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43731901_43731902del , CM000685.2:g.43731901_43731902del	GRCh38
NC_000023.10:g.43591148_43591149del , CM000685.1:g.43591148_43591149del	GRCh37
NC_000023.9:g.43476092_43476093del	NCBI36
NG_008957.2:g.80741_80742del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542639.6:c.556+48_556+49del	ENSP00000440846.1:n.556+48_556+49del
ENST00000686683.1:c.265+48_265+49del	ENSP00000509063.1:n.265+48_265+49del
ENST00000686980.1:n.1087+48_1087+49del
ENST00000688006.1:c.556+48_556+49del	ENSP00000510311.1:n.556+48_556+49del
ENST00000688859.1:n.511+48_511+49del
ENST00000689087.1:c.556+48_556+49del	ENSP00000508997.1:n.556+48_556+49del
ENST00000693128.1:c.850+48_850+49del	ENSP00000508493.1:n.850+48_850+49del
ENST00000338702.4:c.955+48_955+49del MANE Select	ENSP00000340684.3:n.955+48_955+49del
ENST00000338702.3:c.955+48_955+49del	ENSP00000340684.3:n.955+48_955+49del
ENST00000542639.5:c.556+48_556+49del	ENSP00000440846.1:n.556+48_556+49del
NM_000240.3:c.955+48_955+49del	NP_000231.1:n.955+48_955+49del
NM_001270458.1:c.556+48_556+49del	NP_001257387.1:n.556+48_556+49del
NM_000240.4:c.955+48_955+49del MANE Select	NP_000231.1:n.955+48_955+49del
NM_001270458.2:c.556+48_556+49del	NP_001257387.1:n.556+48_556+49del