Canonical Allele Identifier: CA413007667

Gene: MAOA

Linked Data

• MyVariant Identifiers: chrX:g.43590997A>T (hg19) ; chrX:g.43731750A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43731750A>T , CM000685.2:g.43731750A>T	GRCh38
NC_000023.10:g.43590997A>T , CM000685.1:g.43590997A>T	GRCh37
NC_000023.9:g.43475941A>T	NCBI36
NG_008957.2:g.80590A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542639.6:c.453A>T	ENSP00000440846.1:p.Arg151Ser
ENST00000686683.1:c.162A>T	ENSP00000509063.1:p.Arg54Ser
ENST00000686980.1:n.984A>T
ENST00000688006.1:c.453A>T	ENSP00000510311.1:p.Arg151Ser
ENST00000688859.1:n.408A>T
ENST00000689087.1:c.453A>T	ENSP00000508997.1:p.Arg151Ser
ENST00000693128.1:c.747A>T	ENSP00000508493.1:p.Arg249Ser
ENST00000338702.4:c.852A>T MANE Select	ENSP00000340684.3:p.Arg284Ser
ENST00000338702.3:c.852A>T	ENSP00000340684.3:p.Arg284Ser
ENST00000542639.5:c.453A>T	ENSP00000440846.1:p.Arg151Ser
NM_000240.3:c.852A>T	NP_000231.1:p.Arg284Ser
NM_001270458.1:c.453A>T	NP_001257387.1:p.Arg151Ser
NM_000240.4:c.852A>T MANE Select	NP_000231.1:p.Arg284Ser
NM_001270458.2:c.453A>T	NP_001257387.1:p.Arg151Ser