Canonical Allele Identifier: CA2426672392
Gene: MAOA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43740278C= , CM000685.2:g.43740278C= GRCh38
NC_000023.10:g.43599525C= , CM000685.1:g.43599525C= GRCh37
NC_000023.9:g.43484469C= NCBI36
NG_008957.2:g.89118C=

Transcript Alleles

HGVS Amino-acid change
ENST00000542639.6:c.708-403C= ENSP00000440846.1:n.708-403C=
ENST00000686683.1:c.417-403C= ENSP00000509063.1:n.417-403C=
ENST00000686980.1:n.5236C=
ENST00000688006.1:c.708-403C= ENSP00000510311.1:n.708-403C=
ENST00000688859.1:n.663-403C=
ENST00000689087.1:c.708-403C= ENSP00000508997.1:n.708-403C=
ENST00000693128.1:c.1002-403C= ENSP00000508493.1:n.1002-403C=
ENST00000338702.4:c.1107-403C= MANE Select ENSP00000340684.3:n.1107-403C=
ENST00000338702.3:c.1107-403C= ENSP00000340684.3:n.1107-403C=
ENST00000542639.5:c.708-403C= ENSP00000440846.1:n.708-403C=
NM_000240.3:c.1107-403C= NP_000231.1:n.1107-403C=
NM_001270458.1:c.708-403C= NP_001257387.1:n.708-403C=
NM_000240.4:c.1107-403C= MANE Select NP_000231.1:n.1107-403C=
NM_001270458.2:c.708-403C= NP_001257387.1:n.708-403C=