Canonical Allele Identifier: CA329466094

Gene: MAOA

Linked Data

• dbSNP Id: rs1007255740
• gnomAD v3: X-43731550-TG-T
• gnomAD v4: X-43731550-TG-T
• MyVariant Identifiers: chrX:g.43590798del (hg19) ; chrX:g.43731551del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43731551del , CM000685.2:g.43731551del	GRCh38
NC_000023.10:g.43590798del , CM000685.1:g.43590798del	GRCh37
NC_000023.9:g.43475742del	NCBI36
NG_008957.2:g.80391del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542639.6:c.397-143del	ENSP00000440846.1:n.397-143del
ENST00000686683.1:c.106-143del	ENSP00000509063.1:n.106-143del
ENST00000686980.1:n.928-143del
ENST00000688006.1:c.397-143del	ENSP00000510311.1:n.397-143del
ENST00000688859.1:n.352-143del
ENST00000689087.1:c.397-143del	ENSP00000508997.1:n.397-143del
ENST00000693128.1:c.691-143del	ENSP00000508493.1:n.691-143del
ENST00000338702.4:c.796-143del MANE Select	ENSP00000340684.3:n.796-143del
ENST00000338702.3:c.796-143del	ENSP00000340684.3:n.796-143del
ENST00000542639.5:c.397-143del	ENSP00000440846.1:n.397-143del
NM_000240.3:c.796-143del	NP_000231.1:n.796-143del
NM_001270458.1:c.397-143del	NP_001257387.1:n.397-143del
NM_000240.4:c.796-143del MANE Select	NP_000231.1:n.796-143del
NM_001270458.2:c.397-143del	NP_001257387.1:n.397-143del