Canonical Allele Identifier: CA413007365

Gene: MAOA

Linked Data

• MyVariant Identifiers: chrX:g.43590939A>C (hg19) ; chrX:g.43731692A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43731692A>C , CM000685.2:g.43731692A>C	GRCh38
NC_000023.10:g.43590939A>C , CM000685.1:g.43590939A>C	GRCh37
NC_000023.9:g.43475883A>C	NCBI36
NG_008957.2:g.80532A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000542639.6:c.397-2A>C	ENSP00000440846.1:n.397-2A>C
ENST00000686683.1:c.106-2A>C	ENSP00000509063.1:n.106-2A>C
ENST00000686980.1:n.928-2A>C
ENST00000688006.1:c.397-2A>C	ENSP00000510311.1:n.397-2A>C
ENST00000688859.1:n.352-2A>C
ENST00000689087.1:c.397-2A>C	ENSP00000508997.1:n.397-2A>C
ENST00000693128.1:c.691-2A>C	ENSP00000508493.1:n.691-2A>C
ENST00000338702.4:c.796-2A>C MANE Select	ENSP00000340684.3:n.796-2A>C
ENST00000338702.3:c.796-2A>C	ENSP00000340684.3:n.796-2A>C
ENST00000542639.5:c.397-2A>C	ENSP00000440846.1:n.397-2A>C
NM_000240.3:c.796-2A>C	NP_000231.1:n.796-2A>C
NM_001270458.1:c.397-2A>C	NP_001257387.1:n.397-2A>C
NM_000240.4:c.796-2A>C MANE Select	NP_000231.1:n.796-2A>C
NM_001270458.2:c.397-2A>C	NP_001257387.1:n.397-2A>C