Canonical Allele Identifier: CA2426672907
Gene: MAOA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43741895C= , CM000685.2:g.43741895C= GRCh38
NC_000023.10:g.43601142C= , CM000685.1:g.43601142C= GRCh37
NC_000023.9:g.43486086C= NCBI36
NG_008957.2:g.90735C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000542639.6:c.766-55C= ENSP00000440846.1:n.766-55C=
ENST00000686683.1:c.475-55C= ENSP00000509063.1:n.475-55C=
ENST00000686980.1:n.5697-55C=
ENST00000688006.1:c.766-55C= ENSP00000510311.1:n.766-55C=
ENST00000688859.1:n.721-55C=
ENST00000689087.1:c.766-55C= ENSP00000508997.1:n.766-55C=
ENST00000693128.1:c.1060-55C= ENSP00000508493.1:n.1060-55C=
ENST00000338702.4:c.1165-55C= MANE Select ENSP00000340684.3:n.1165-55C=
ENST00000338702.3:c.1165-55C= ENSP00000340684.3:n.1165-55C=
ENST00000542639.5:c.766-55C= ENSP00000440846.1:n.766-55C=
NM_000240.3:c.1165-55C= NP_000231.1:n.1165-55C=
NM_001270458.1:c.766-55C= NP_001257387.1:n.766-55C=
NM_000240.4:c.1165-55C= MANE Select NP_000231.1:n.1165-55C=
NM_001270458.2:c.766-55C= NP_001257387.1:n.766-55C=