Canonical Allele Identifier: CA413007419

Gene: MAOA

Linked Data

• MyVariant Identifiers: chrX:g.43590947T>C (hg19) ; chrX:g.43731700T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43731700T>C , CM000685.2:g.43731700T>C	GRCh38
NC_000023.10:g.43590947T>C , CM000685.1:g.43590947T>C	GRCh37
NC_000023.9:g.43475891T>C	NCBI36
NG_008957.2:g.80540T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000542639.6:c.403T>C	ENSP00000440846.1:p.Tyr135His
ENST00000686683.1:c.112T>C	ENSP00000509063.1:p.Tyr38His
ENST00000686980.1:n.934T>C
ENST00000688006.1:c.403T>C	ENSP00000510311.1:p.Tyr135His
ENST00000688859.1:n.358T>C
ENST00000689087.1:c.403T>C	ENSP00000508997.1:p.Tyr135His
ENST00000693128.1:c.697T>C	ENSP00000508493.1:p.Tyr233His
ENST00000338702.4:c.802T>C MANE Select	ENSP00000340684.3:p.Tyr268His
ENST00000338702.3:c.802T>C	ENSP00000340684.3:p.Tyr268His
ENST00000542639.5:c.403T>C	ENSP00000440846.1:p.Tyr135His
NM_000240.3:c.802T>C	NP_000231.1:p.Tyr268His
NM_001270458.1:c.403T>C	NP_001257387.1:p.Tyr135His
NM_000240.4:c.802T>C MANE Select	NP_000231.1:p.Tyr268His
NM_001270458.2:c.403T>C	NP_001257387.1:p.Tyr135His