Canonical Allele Identifier: CA875555138

Gene: MAOA

Linked Data

• dbSNP Id: rs1264002318
• MyVariant Identifiers: chrX:g.43591130T>C (hg19) ; chrX:g.43731883T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43731883T>C , CM000685.2:g.43731883T>C	GRCh38
NC_000023.10:g.43591130T>C , CM000685.1:g.43591130T>C	GRCh37
NC_000023.9:g.43476074T>C	NCBI36
NG_008957.2:g.80723T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542639.6:c.556+30T>C	ENSP00000440846.1:n.556+30T>C
ENST00000686683.1:c.265+30T>C	ENSP00000509063.1:n.265+30T>C
ENST00000686980.1:n.1087+30T>C
ENST00000688006.1:c.556+30T>C	ENSP00000510311.1:n.556+30T>C
ENST00000688859.1:n.511+30T>C
ENST00000689087.1:c.556+30T>C	ENSP00000508997.1:n.556+30T>C
ENST00000693128.1:c.850+30T>C	ENSP00000508493.1:n.850+30T>C
ENST00000338702.4:c.955+30T>C MANE Select	ENSP00000340684.3:n.955+30T>C
ENST00000338702.3:c.955+30T>C	ENSP00000340684.3:n.955+30T>C
ENST00000542639.5:c.556+30T>C	ENSP00000440846.1:n.556+30T>C
NM_000240.3:c.955+30T>C	NP_000231.1:n.955+30T>C
NM_001270458.1:c.556+30T>C	NP_001257387.1:n.556+30T>C
NM_000240.4:c.955+30T>C MANE Select	NP_000231.1:n.955+30T>C
NM_001270458.2:c.556+30T>C	NP_001257387.1:n.556+30T>C