Canonical Allele Identifier: CA413007368
Gene: MAOA HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

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