Canonical Allele Identifier: CA413008255

Gene: MAOA

Linked Data

• dbSNP Id: rs2033884280
• MyVariant Identifiers: chrX:g.43591076A>C (hg19) ; chrX:g.43731829A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43731829A>C , CM000685.2:g.43731829A>C	GRCh38
NC_000023.10:g.43591076A>C , CM000685.1:g.43591076A>C	GRCh37
NC_000023.9:g.43476020A>C	NCBI36
NG_008957.2:g.80669A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542639.6:c.532A>C	ENSP00000440846.1:p.Lys178Gln
ENST00000686683.1:c.241A>C	ENSP00000509063.1:p.Lys81Gln
ENST00000686980.1:n.1063A>C
ENST00000688006.1:c.532A>C	ENSP00000510311.1:p.Lys178Gln
ENST00000688859.1:n.487A>C
ENST00000689087.1:c.532A>C	ENSP00000508997.1:p.Lys178Gln
ENST00000693128.1:c.826A>C	ENSP00000508493.1:p.Lys276Gln
ENST00000338702.4:c.931A>C MANE Select	ENSP00000340684.3:p.Lys311Gln
ENST00000338702.3:c.931A>C	ENSP00000340684.3:p.Lys311Gln
ENST00000542639.5:c.532A>C	ENSP00000440846.1:p.Lys178Gln
NM_000240.3:c.931A>C	NP_000231.1:p.Lys311Gln
NM_001270458.1:c.532A>C	NP_001257387.1:p.Lys178Gln
NM_000240.4:c.931A>C MANE Select	NP_000231.1:p.Lys311Gln
NM_001270458.2:c.532A>C	NP_001257387.1:p.Lys178Gln