Canonical Allele Identifier: CA413007451

Gene: MAOA

Linked Data

• MyVariant Identifiers: chrX:g.43590953A>C (hg19) ; chrX:g.43731706A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43731706A>C , CM000685.2:g.43731706A>C	GRCh38
NC_000023.10:g.43590953A>C , CM000685.1:g.43590953A>C	GRCh37
NC_000023.9:g.43475897A>C	NCBI36
NG_008957.2:g.80546A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000542639.6:c.409A>C	ENSP00000440846.1:p.Ile137Leu
ENST00000686683.1:c.118A>C	ENSP00000509063.1:p.Ile40Leu
ENST00000686980.1:n.940A>C
ENST00000688006.1:c.409A>C	ENSP00000510311.1:p.Ile137Leu
ENST00000688859.1:n.364A>C
ENST00000689087.1:c.409A>C	ENSP00000508997.1:p.Ile137Leu
ENST00000693128.1:c.703A>C	ENSP00000508493.1:p.Ile235Leu
ENST00000338702.4:c.808A>C MANE Select	ENSP00000340684.3:p.Ile270Leu
ENST00000338702.3:c.808A>C	ENSP00000340684.3:p.Ile270Leu
ENST00000542639.5:c.409A>C	ENSP00000440846.1:p.Ile137Leu
NM_000240.3:c.808A>C	NP_000231.1:p.Ile270Leu
NM_001270458.1:c.409A>C	NP_001257387.1:p.Ile137Leu
NM_000240.4:c.808A>C MANE Select	NP_000231.1:p.Ile270Leu
NM_001270458.2:c.409A>C	NP_001257387.1:p.Ile137Leu