Canonical Allele Identifier: CA413008369

Gene: MAOA

Linked Data

• gnomAD v4: X-43731851-A-C
• MyVariant Identifiers: chrX:g.43591098A>C (hg19) ; chrX:g.43731851A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43731851A>C , CM000685.2:g.43731851A>C	GRCh38
NC_000023.10:g.43591098A>C , CM000685.1:g.43591098A>C	GRCh37
NC_000023.9:g.43476042A>C	NCBI36
NG_008957.2:g.80691A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542639.6:c.554A>C	ENSP00000440846.1:p.Lys185Thr
ENST00000686683.1:c.263A>C	ENSP00000509063.1:p.Lys88Thr
ENST00000686980.1:n.1085A>C
ENST00000688006.1:c.554A>C	ENSP00000510311.1:p.Lys185Thr
ENST00000688859.1:n.509A>C
ENST00000689087.1:c.554A>C	ENSP00000508997.1:p.Lys185Thr
ENST00000693128.1:c.848A>C	ENSP00000508493.1:p.Lys283Thr
ENST00000338702.4:c.953A>C MANE Select	ENSP00000340684.3:p.Lys318Thr
ENST00000338702.3:c.953A>C	ENSP00000340684.3:p.Lys318Thr
ENST00000542639.5:c.554A>C	ENSP00000440846.1:p.Lys185Thr
NM_000240.3:c.953A>C	NP_000231.1:p.Lys318Thr
NM_001270458.1:c.554A>C	NP_001257387.1:p.Lys185Thr
NM_000240.4:c.953A>C MANE Select	NP_000231.1:p.Lys318Thr
NM_001270458.2:c.554A>C	NP_001257387.1:p.Lys185Thr