Canonical Allele Identifier: CA413007459

Gene: MAOA

Linked Data

• MyVariant Identifiers: chrX:g.43590954T>C (hg19) ; chrX:g.43731707T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43731707T>C , CM000685.2:g.43731707T>C	GRCh38
NC_000023.10:g.43590954T>C , CM000685.1:g.43590954T>C	GRCh37
NC_000023.9:g.43475898T>C	NCBI36
NG_008957.2:g.80547T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542639.6:c.410T>C	ENSP00000440846.1:p.Ile137Thr
ENST00000686683.1:c.119T>C	ENSP00000509063.1:p.Ile40Thr
ENST00000686980.1:n.941T>C
ENST00000688006.1:c.410T>C	ENSP00000510311.1:p.Ile137Thr
ENST00000688859.1:n.365T>C
ENST00000689087.1:c.410T>C	ENSP00000508997.1:p.Ile137Thr
ENST00000693128.1:c.704T>C	ENSP00000508493.1:p.Ile235Thr
ENST00000338702.4:c.809T>C MANE Select	ENSP00000340684.3:p.Ile270Thr
ENST00000338702.3:c.809T>C	ENSP00000340684.3:p.Ile270Thr
ENST00000542639.5:c.410T>C	ENSP00000440846.1:p.Ile137Thr
NM_000240.3:c.809T>C	NP_000231.1:p.Ile270Thr
NM_001270458.1:c.410T>C	NP_001257387.1:p.Ile137Thr
NM_000240.4:c.809T>C MANE Select	NP_000231.1:p.Ile270Thr
NM_001270458.2:c.410T>C	NP_001257387.1:p.Ile137Thr