Canonical Allele Identifier: CA413008128

Gene: MAOA

Linked Data

• MyVariant Identifiers: chrX:g.43591049G>C (hg19) ; chrX:g.43731802G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43731802G>C , CM000685.2:g.43731802G>C	GRCh38
NC_000023.10:g.43591049G>C , CM000685.1:g.43591049G>C	GRCh37
NC_000023.9:g.43475993G>C	NCBI36
NG_008957.2:g.80642G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000542639.6:c.505G>C	ENSP00000440846.1:p.Ala169Pro
ENST00000686683.1:c.214G>C	ENSP00000509063.1:p.Ala72Pro
ENST00000686980.1:n.1036G>C
ENST00000688006.1:c.505G>C	ENSP00000510311.1:p.Ala169Pro
ENST00000688859.1:n.460G>C
ENST00000689087.1:c.505G>C	ENSP00000508997.1:p.Ala169Pro
ENST00000693128.1:c.799G>C	ENSP00000508493.1:p.Ala267Pro
ENST00000338702.4:c.904G>C MANE Select	ENSP00000340684.3:p.Ala302Pro
ENST00000338702.3:c.904G>C	ENSP00000340684.3:p.Ala302Pro
ENST00000542639.5:c.505G>C	ENSP00000440846.1:p.Ala169Pro
NM_000240.3:c.904G>C	NP_000231.1:p.Ala302Pro
NM_001270458.1:c.505G>C	NP_001257387.1:p.Ala169Pro
NM_000240.4:c.904G>C MANE Select	NP_000231.1:p.Ala302Pro
NM_001270458.2:c.505G>C	NP_001257387.1:p.Ala169Pro