Canonical Allele Identifier: CA10390839

Gene: MAOA

Linked Data

• dbSNP Id: rs776818874
• ExAC: X:43590926 TTG / T
• gnomAD v2: X-43590926-TTG-T
• gnomAD v4: X-43731679-TTG-T
• MyVariant Identifiers: chrX:g.43590927_43590928del (hg19) ; chrX:g.43731680_43731681del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43731687_43731688del , CM000685.2:g.43731687_43731688del	GRCh38
NC_000023.10:g.43590934_43590935del , CM000685.1:g.43590934_43590935del	GRCh37
NC_000023.9:g.43475878_43475879del	NCBI36
NG_008957.2:g.80527_80528del

Transcript Alleles

HGVS	Amino-acid change
ENST00000542639.6:c.397-7_397-6del	ENSP00000440846.1:n.397-7_397-6del
ENST00000686683.1:c.106-7_106-6del	ENSP00000509063.1:n.106-7_106-6del
ENST00000686980.1:n.928-7_928-6del
ENST00000688006.1:c.397-7_397-6del	ENSP00000510311.1:n.397-7_397-6del
ENST00000688859.1:n.352-7_352-6del
ENST00000689087.1:c.397-7_397-6del	ENSP00000508997.1:n.397-7_397-6del
ENST00000693128.1:c.691-7_691-6del	ENSP00000508493.1:n.691-7_691-6del
ENST00000338702.4:c.796-7_796-6del MANE Select	ENSP00000340684.3:n.796-7_796-6del
ENST00000338702.3:c.796-7_796-6del	ENSP00000340684.3:n.796-7_796-6del
ENST00000542639.5:c.397-7_397-6del	ENSP00000440846.1:n.397-7_397-6del
NM_000240.3:c.796-7_796-6del	NP_000231.1:n.796-7_796-6del
NM_001270458.1:c.397-7_397-6del	NP_001257387.1:n.397-7_397-6del
NM_000240.4:c.796-7_796-6del MANE Select	NP_000231.1:n.796-7_796-6del
NM_001270458.2:c.397-7_397-6del	NP_001257387.1:n.397-7_397-6del