Canonical Allele Identifier: CA516138080

Gene: MAOA

Linked Data

• MyVariant Identifiers: chrX:g.43590946A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43731699A>G , CM000685.2:g.43731699A>G	GRCh38
NC_000023.10:g.43590946A>G , CM000685.1:g.43590946A>G	GRCh37
NC_000023.9:g.43475890A>G	NCBI36
NG_008957.2:g.80539A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542639.6:c.402A>G	ENSP00000440846.1:p.Lys134=
ENST00000686683.1:c.111A>G	ENSP00000509063.1:p.Lys37=
ENST00000686980.1:n.933A>G
ENST00000688006.1:c.402A>G	ENSP00000510311.1:p.Lys134=
ENST00000688859.1:n.357A>G
ENST00000689087.1:c.402A>G	ENSP00000508997.1:p.Lys134=
ENST00000693128.1:c.696A>G	ENSP00000508493.1:p.Lys232=
ENST00000338702.4:c.801A>G MANE Select	ENSP00000340684.3:p.Lys267=
ENST00000338702.3:c.801A>G	ENSP00000340684.3:p.Lys267=
ENST00000542639.5:c.402A>G	ENSP00000440846.1:p.Lys134=
NM_000240.3:c.801A>G	NP_000231.1:p.Lys267=
NM_001270458.1:c.402A>G	NP_001257387.1:p.Lys134=
NM_000240.4:c.801A>G MANE Select	NP_000231.1:p.Lys267=
NM_001270458.2:c.402A>G	NP_001257387.1:p.Lys134=