Canonical Allele Identifier: CA2695233737

Gene: MAOA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43731695_43731696delinsTT , CM000685.2:g.43731695_43731696delinsTT	GRCh38
NC_000023.10:g.43590942_43590943delinsTT , CM000685.1:g.43590942_43590943delinsTT	GRCh37
NC_000023.9:g.43475886_43475887delinsTT	NCBI36
NG_008957.2:g.80535_80536delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542639.6:c.398_399delinsTT	ENSP00000440846.1:p.Cys133Phe
ENST00000686683.1:c.107_108delinsTT	ENSP00000509063.1:p.Cys36Phe
ENST00000686980.1:n.929_930delinsTT
ENST00000688006.1:c.398_399delinsTT	ENSP00000510311.1:p.Cys133Phe
ENST00000688859.1:n.353_354delinsTT
ENST00000689087.1:c.398_399delinsTT	ENSP00000508997.1:p.Cys133Phe
ENST00000693128.1:c.692_693delinsTT	ENSP00000508493.1:p.Cys231Phe
ENST00000338702.4:c.797_798delinsTT MANE Select	ENSP00000340684.3:p.Cys266Phe
ENST00000338702.3:c.797_798delinsTT	ENSP00000340684.3:p.Cys266Phe
ENST00000542639.5:c.398_399delinsTT	ENSP00000440846.1:p.Cys133Phe
NM_000240.3:c.797_798delinsTT	NP_000231.1:p.Cys266Phe
NM_001270458.1:c.398_399delinsTT	NP_001257387.1:p.Cys133Phe
NM_000240.4:c.797_798delinsTT MANE Select	NP_000231.1:p.Cys266Phe
NM_001270458.2:c.398_399delinsTT	NP_001257387.1:p.Cys133Phe