Canonical Allele Identifier: CA413008198

Gene: MAOA

Linked Data

• MyVariant Identifiers: chrX:g.43591064A>C (hg19) ; chrX:g.43731817A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43731817A>C , CM000685.2:g.43731817A>C	GRCh38
NC_000023.10:g.43591064A>C , CM000685.1:g.43591064A>C	GRCh37
NC_000023.9:g.43476008A>C	NCBI36
NG_008957.2:g.80657A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542639.6:c.520A>C	ENSP00000440846.1:p.Met174Leu
ENST00000686683.1:c.229A>C	ENSP00000509063.1:p.Met77Leu
ENST00000686980.1:n.1051A>C
ENST00000688006.1:c.520A>C	ENSP00000510311.1:p.Met174Leu
ENST00000688859.1:n.475A>C
ENST00000689087.1:c.520A>C	ENSP00000508997.1:p.Met174Leu
ENST00000693128.1:c.814A>C	ENSP00000508493.1:p.Met272Leu
ENST00000338702.4:c.919A>C MANE Select	ENSP00000340684.3:p.Met307Leu
ENST00000338702.3:c.919A>C	ENSP00000340684.3:p.Met307Leu
ENST00000542639.5:c.520A>C	ENSP00000440846.1:p.Met174Leu
NM_000240.3:c.919A>C	NP_000231.1:p.Met307Leu
NM_001270458.1:c.520A>C	NP_001257387.1:p.Met174Leu
NM_000240.4:c.919A>C MANE Select	NP_000231.1:p.Met307Leu
NM_001270458.2:c.520A>C	NP_001257387.1:p.Met174Leu