Canonical Allele Identifier: CA2426669453

Gene: MAOA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43731828C= , CM000685.2:g.43731828C=	GRCh38
NC_000023.10:g.43591075C= , CM000685.1:g.43591075C=	GRCh37
NC_000023.9:g.43476019C=	NCBI36
NG_008957.2:g.80668C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542639.6:c.531C=	ENSP00000440846.1:p.Tyr177=
ENST00000686683.1:c.240C=	ENSP00000509063.1:p.Tyr80=
ENST00000686980.1:n.1062C=
ENST00000688006.1:c.531C=	ENSP00000510311.1:p.Tyr177=
ENST00000688859.1:n.486C=
ENST00000689087.1:c.531C=	ENSP00000508997.1:p.Tyr177=
ENST00000693128.1:c.825C=	ENSP00000508493.1:p.Tyr275=
ENST00000338702.4:c.930C= MANE Select	ENSP00000340684.3:p.Tyr310=
ENST00000338702.3:c.930C=	ENSP00000340684.3:p.Tyr310=
ENST00000542639.5:c.531C=	ENSP00000440846.1:p.Tyr177=
NM_000240.3:c.930C=	NP_000231.1:p.Tyr310=
NM_001270458.1:c.531C=	NP_001257387.1:p.Tyr177=
NM_000240.4:c.930C= MANE Select	NP_000231.1:p.Tyr310=
NM_001270458.2:c.531C=	NP_001257387.1:p.Tyr177=