Canonical Allele Identifier: CA2426672397

Gene: MAOA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43740288_43740289delinsAT , CM000685.2:g.43740288_43740289delinsAT	GRCh38
NC_000023.10:g.43599535_43599536delinsAT , CM000685.1:g.43599535_43599536delinsAT	GRCh37
NC_000023.9:g.43484479_43484480delinsAT	NCBI36
NG_008957.2:g.89128_89129delinsAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000542639.6:c.708-393_708-392delinsAT	ENSP00000440846.1:n.708-393_708-392delins...
ENST00000686683.1:c.417-393_417-392delinsAT	ENSP00000509063.1:n.417-393_417-392delins...
ENST00000686980.1:n.5246_5247delinsAT
ENST00000688006.1:c.708-393_708-392delinsAT	ENSP00000510311.1:n.708-393_708-392delins...
ENST00000688859.1:n.663-393_663-392delinsAT
ENST00000689087.1:c.708-393_708-392delinsAT	ENSP00000508997.1:n.708-393_708-392delins...
ENST00000693128.1:c.1002-393_1002-392delinsAT	ENSP00000508493.1:n.1002-393_1002-392deli...
ENST00000338702.4:c.1107-393_1107-392delinsAT MANE Select	ENSP00000340684.3:n.1107-393_1107-392deli...
ENST00000338702.3:c.1107-393_1107-392delinsAT	ENSP00000340684.3:n.1107-393_1107-392deli...
ENST00000542639.5:c.708-393_708-392delinsAT	ENSP00000440846.1:n.708-393_708-392delins...
NM_000240.3:c.1107-393_1107-392delinsAT	NP_000231.1:n.1107-393_1107-392delinsAT
NM_001270458.1:c.708-393_708-392delinsAT	NP_001257387.1:n.708-393_708-392delinsAT
NM_000240.4:c.1107-393_1107-392delinsAT MANE Select	NP_000231.1:n.1107-393_1107-392delinsAT
NM_001270458.2:c.708-393_708-392delinsAT	NP_001257387.1:n.708-393_708-392delinsAT