Canonical Allele Identifier: CA2426670381

Gene: MAOA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43733516T= , CM000685.2:g.43733516T=	GRCh38
NC_000023.10:g.43592763T= , CM000685.1:g.43592763T=	GRCh37
NC_000023.9:g.43477707T=	NCBI36
NG_008957.2:g.82356T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542639.6:c.653+721T=	ENSP00000440846.1:n.653+721T=
ENST00000686683.1:c.362+721T=	ENSP00000509063.1:n.362+721T=
ENST00000686980.1:n.1184+721T=
ENST00000688006.1:c.653+721T=	ENSP00000510311.1:n.653+721T=
ENST00000688859.1:n.608+721T=
ENST00000689087.1:c.653+721T=	ENSP00000508997.1:n.653+721T=
ENST00000693128.1:c.947+721T=	ENSP00000508493.1:n.947+721T=
ENST00000338702.4:c.1052+721T= MANE Select	ENSP00000340684.3:n.1052+721T=
ENST00000338702.3:c.1052+721T=	ENSP00000340684.3:n.1052+721T=
ENST00000542639.5:c.653+721T=	ENSP00000440846.1:n.653+721T=
NM_000240.3:c.1052+721T=	NP_000231.1:n.1052+721T=
NM_001270458.1:c.653+721T=	NP_001257387.1:n.653+721T=
NM_000240.4:c.1052+721T= MANE Select	NP_000231.1:n.1052+721T=
NM_001270458.2:c.653+721T=	NP_001257387.1:n.653+721T=