Canonical Allele Identifier: CA329466113

Gene: MAOA

Linked Data

• dbSNP Id: rs139718660
• gnomAD v2: X-43591231-G-T
• gnomAD v3: X-43731984-G-T
• gnomAD v4: X-43731984-G-T
• MyVariant Identifiers: chrX:g.43591231G>T (hg19) ; chrX:g.43731984G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43731984G>T , CM000685.2:g.43731984G>T	GRCh38
NC_000023.10:g.43591231G>T , CM000685.1:g.43591231G>T	GRCh37
NC_000023.9:g.43476175G>T	NCBI36
NG_008957.2:g.80824G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542639.6:c.556+131G>T	ENSP00000440846.1:n.556+131G>T
ENST00000686683.1:c.265+131G>T	ENSP00000509063.1:n.265+131G>T
ENST00000686980.1:n.1087+131G>T
ENST00000688006.1:c.556+131G>T	ENSP00000510311.1:n.556+131G>T
ENST00000688859.1:n.511+131G>T
ENST00000689087.1:c.556+131G>T	ENSP00000508997.1:n.556+131G>T
ENST00000693128.1:c.850+131G>T	ENSP00000508493.1:n.850+131G>T
ENST00000338702.4:c.955+131G>T MANE Select	ENSP00000340684.3:n.955+131G>T
ENST00000338702.3:c.955+131G>T	ENSP00000340684.3:n.955+131G>T
ENST00000542639.5:c.556+131G>T	ENSP00000440846.1:n.556+131G>T
NM_000240.3:c.955+131G>T	NP_000231.1:n.955+131G>T
NM_001270458.1:c.556+131G>T	NP_001257387.1:n.556+131G>T
NM_000240.4:c.955+131G>T MANE Select	NP_000231.1:n.955+131G>T
NM_001270458.2:c.556+131G>T	NP_001257387.1:n.556+131G>T