Canonical Allele Identifier: CA413007625

Gene: MAOA

Linked Data

• MyVariant Identifiers: chrX:g.43590989C>T (hg19) ; chrX:g.43731742C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43731742C>T , CM000685.2:g.43731742C>T	GRCh38
NC_000023.10:g.43590989C>T , CM000685.1:g.43590989C>T	GRCh37
NC_000023.9:g.43475933C>T	NCBI36
NG_008957.2:g.80582C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542639.6:c.445C>T	ENSP00000440846.1:p.His149Tyr
ENST00000686683.1:c.154C>T	ENSP00000509063.1:p.His52Tyr
ENST00000686980.1:n.976C>T
ENST00000688006.1:c.445C>T	ENSP00000510311.1:p.His149Tyr
ENST00000688859.1:n.400C>T
ENST00000689087.1:c.445C>T	ENSP00000508997.1:p.His149Tyr
ENST00000693128.1:c.739C>T	ENSP00000508493.1:p.His247Tyr
ENST00000338702.4:c.844C>T MANE Select	ENSP00000340684.3:p.His282Tyr
ENST00000338702.3:c.844C>T	ENSP00000340684.3:p.His282Tyr
ENST00000542639.5:c.445C>T	ENSP00000440846.1:p.His149Tyr
NM_000240.3:c.844C>T	NP_000231.1:p.His282Tyr
NM_001270458.1:c.445C>T	NP_001257387.1:p.His149Tyr
NM_000240.4:c.844C>T MANE Select	NP_000231.1:p.His282Tyr
NM_001270458.2:c.445C>T	NP_001257387.1:p.His149Tyr