Canonical Allele Identifier: CA2426672399
Gene: MAOA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43740291A= , CM000685.2:g.43740291A= GRCh38
NC_000023.10:g.43599538A= , CM000685.1:g.43599538A= GRCh37
NC_000023.9:g.43484482A= NCBI36
NG_008957.2:g.89131A=

Transcript Alleles

HGVS Amino-acid change
ENST00000542639.6:c.708-390A= ENSP00000440846.1:n.708-390A=
ENST00000686683.1:c.417-390A= ENSP00000509063.1:n.417-390A=
ENST00000686980.1:n.5249A=
ENST00000688006.1:c.708-390A= ENSP00000510311.1:n.708-390A=
ENST00000688859.1:n.663-390A=
ENST00000689087.1:c.708-390A= ENSP00000508997.1:n.708-390A=
ENST00000693128.1:c.1002-390A= ENSP00000508493.1:n.1002-390A=
ENST00000338702.4:c.1107-390A= MANE Select ENSP00000340684.3:n.1107-390A=
ENST00000338702.3:c.1107-390A= ENSP00000340684.3:n.1107-390A=
ENST00000542639.5:c.708-390A= ENSP00000440846.1:n.708-390A=
NM_000240.3:c.1107-390A= NP_000231.1:n.1107-390A=
NM_001270458.1:c.708-390A= NP_001257387.1:n.708-390A=
NM_000240.4:c.1107-390A= MANE Select NP_000231.1:n.1107-390A=
NM_001270458.2:c.708-390A= NP_001257387.1:n.708-390A=