Canonical Allele Identifier: CA413007960

Gene: MAOA

Linked Data

• MyVariant Identifiers: chrX:g.43591029T>C (hg19) ; chrX:g.43731782T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43731782T>C , CM000685.2:g.43731782T>C	GRCh38
NC_000023.10:g.43591029T>C , CM000685.1:g.43591029T>C	GRCh37
NC_000023.9:g.43475973T>C	NCBI36
NG_008957.2:g.80622T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542639.6:c.485T>C	ENSP00000440846.1:p.Ile162Thr
ENST00000686683.1:c.194T>C	ENSP00000509063.1:p.Ile65Thr
ENST00000686980.1:n.1016T>C
ENST00000688006.1:c.485T>C	ENSP00000510311.1:p.Ile162Thr
ENST00000688859.1:n.440T>C
ENST00000689087.1:c.485T>C	ENSP00000508997.1:p.Ile162Thr
ENST00000693128.1:c.779T>C	ENSP00000508493.1:p.Ile260Thr
ENST00000338702.4:c.884T>C MANE Select	ENSP00000340684.3:p.Ile295Thr
ENST00000338702.3:c.884T>C	ENSP00000340684.3:p.Ile295Thr
ENST00000542639.5:c.485T>C	ENSP00000440846.1:p.Ile162Thr
NM_000240.3:c.884T>C	NP_000231.1:p.Ile295Thr
NM_001270458.1:c.485T>C	NP_001257387.1:p.Ile162Thr
NM_000240.4:c.884T>C MANE Select	NP_000231.1:p.Ile295Thr
NM_001270458.2:c.485T>C	NP_001257387.1:p.Ile162Thr