Canonical Allele Identifier: CA2426669473

Gene: MAOA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43731898_43731900delinsTCA , CM000685.2:g.43731898_43731900delinsTCA	GRCh38
NC_000023.10:g.43591145_43591147delinsTCA , CM000685.1:g.43591145_43591147delinsTCA	GRCh37
NC_000023.9:g.43476089_43476091delinsTCA	NCBI36
NG_008957.2:g.80738_80740delinsTCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542639.6:c.556+45_556+47delinsTCA	ENSP00000440846.1:n.556+45_556+47delinsTCA
ENST00000686683.1:c.265+45_265+47delinsTCA	ENSP00000509063.1:n.265+45_265+47delinsTCA
ENST00000686980.1:n.1087+45_1087+47delinsTCA
ENST00000688006.1:c.556+45_556+47delinsTCA	ENSP00000510311.1:n.556+45_556+47delinsTCA
ENST00000688859.1:n.511+45_511+47delinsTCA
ENST00000689087.1:c.556+45_556+47delinsTCA	ENSP00000508997.1:n.556+45_556+47delinsTCA
ENST00000693128.1:c.850+45_850+47delinsTCA	ENSP00000508493.1:n.850+45_850+47delinsTCA
ENST00000338702.4:c.955+45_955+47delinsTCA MANE Select	ENSP00000340684.3:n.955+45_955+47delinsTCA
ENST00000338702.3:c.955+45_955+47delinsTCA	ENSP00000340684.3:n.955+45_955+47delinsTCA
ENST00000542639.5:c.556+45_556+47delinsTCA	ENSP00000440846.1:n.556+45_556+47delinsTCA
NM_000240.3:c.955+45_955+47delinsTCA	NP_000231.1:n.955+45_955+47delinsTCA
NM_001270458.1:c.556+45_556+47delinsTCA	NP_001257387.1:n.556+45_556+47delinsTCA
NM_000240.4:c.955+45_955+47delinsTCA MANE Select	NP_000231.1:n.955+45_955+47delinsTCA
NM_001270458.2:c.556+45_556+47delinsTCA	NP_001257387.1:n.556+45_556+47delinsTCA