Canonical Allele Identifier: CA329463396

Gene: MAOA

Linked Data

• dbSNP Id: rs942323669
• MyVariant Identifiers: chrX:g.43553220C>A (hg19) ; chrX:g.43693973C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43693973C>A , CM000685.2:g.43693973C>A	GRCh38
NC_000023.10:g.43553220C>A , CM000685.1:g.43553220C>A	GRCh37
NC_000023.9:g.43438164C>A	NCBI36
NG_008957.2:g.42813C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000497485.2:n.983C>A
ENST00000542639.6:c.-94+545C>A	ENSP00000440846.1:n.-94+545C>A
ENST00000686683.1:c.-305+545C>A	ENSP00000509063.1:n.-305+545C>A
ENST00000686980.1:n.438+545C>A
ENST00000688006.1:c.-94+545C>A	ENSP00000510311.1:n.-94+545C>A
ENST00000689087.1:c.-94+545C>A	ENSP00000508997.1:n.-94+545C>A
ENST00000693128.1:c.306+545C>A	ENSP00000508493.1:n.306+545C>A
ENST00000338702.4:c.306+545C>A MANE Select	ENSP00000340684.3:n.306+545C>A
ENST00000338702.3:c.306+545C>A	ENSP00000340684.3:n.306+545C>A
ENST00000497485.1:n.454+545C>A
ENST00000542639.5:c.-94+545C>A	ENSP00000440846.1:n.-94+545C>A
NM_000240.3:c.306+545C>A	NP_000231.1:n.306+545C>A
NM_001270458.1:c.-94+545C>A	NP_001257387.1:n.-94+545C>A
NM_000240.4:c.306+545C>A MANE Select	NP_000231.1:n.306+545C>A
NM_001270458.2:c.-94+545C>A	NP_001257387.1:n.-94+545C>A