Canonical Allele Identifier: CA413007659

Gene: MAOA

Linked Data

• MyVariant Identifiers: chrX:g.43590996G>C (hg19) ; chrX:g.43731749G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43731749G>C , CM000685.2:g.43731749G>C	GRCh38
NC_000023.10:g.43590996G>C , CM000685.1:g.43590996G>C	GRCh37
NC_000023.9:g.43475940G>C	NCBI36
NG_008957.2:g.80589G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542639.6:c.452G>C	ENSP00000440846.1:p.Arg151Thr
ENST00000686683.1:c.161G>C	ENSP00000509063.1:p.Arg54Thr
ENST00000686980.1:n.983G>C
ENST00000688006.1:c.452G>C	ENSP00000510311.1:p.Arg151Thr
ENST00000688859.1:n.407G>C
ENST00000689087.1:c.452G>C	ENSP00000508997.1:p.Arg151Thr
ENST00000693128.1:c.746G>C	ENSP00000508493.1:p.Arg249Thr
ENST00000338702.4:c.851G>C MANE Select	ENSP00000340684.3:p.Arg284Thr
ENST00000338702.3:c.851G>C	ENSP00000340684.3:p.Arg284Thr
ENST00000542639.5:c.452G>C	ENSP00000440846.1:p.Arg151Thr
NM_000240.3:c.851G>C	NP_000231.1:p.Arg284Thr
NM_001270458.1:c.452G>C	NP_001257387.1:p.Arg151Thr
NM_000240.4:c.851G>C MANE Select	NP_000231.1:p.Arg284Thr
NM_001270458.2:c.452G>C	NP_001257387.1:p.Arg151Thr