Canonical Allele Identifier: CA516138086

Gene: MAOA

Linked Data

• MyVariant Identifiers: chrX:g.43590958T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43731711T>C , CM000685.2:g.43731711T>C	GRCh38
NC_000023.10:g.43590958T>C , CM000685.1:g.43590958T>C	GRCh37
NC_000023.9:g.43475902T>C	NCBI36
NG_008957.2:g.80551T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542639.6:c.414T>C	ENSP00000440846.1:p.Asn138=
ENST00000686683.1:c.123T>C	ENSP00000509063.1:p.Asn41=
ENST00000686980.1:n.945T>C
ENST00000688006.1:c.414T>C	ENSP00000510311.1:p.Asn138=
ENST00000688859.1:n.369T>C
ENST00000689087.1:c.414T>C	ENSP00000508997.1:p.Asn138=
ENST00000693128.1:c.708T>C	ENSP00000508493.1:p.Asn236=
ENST00000338702.4:c.813T>C MANE Select	ENSP00000340684.3:p.Asn271=
ENST00000338702.3:c.813T>C	ENSP00000340684.3:p.Asn271=
ENST00000542639.5:c.414T>C	ENSP00000440846.1:p.Asn138=
NM_000240.3:c.813T>C	NP_000231.1:p.Asn271=
NM_001270458.1:c.414T>C	NP_001257387.1:p.Asn138=
NM_000240.4:c.813T>C MANE Select	NP_000231.1:p.Asn271=
NM_001270458.2:c.414T>C	NP_001257387.1:p.Asn138=