Canonical Allele Identifier: CA2426652907
Gene: MAOA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43678769A= , CM000685.2:g.43678769A= GRCh38
NC_000023.10:g.43538017A= , CM000685.1:g.43538017A= GRCh37
NC_000023.9:g.43422961A= NCBI36
NG_008957.2:g.27609A=

Transcript Alleles

HGVS Amino-acid Change
NM_000240.4:c.74-4744A= MANE Select NP_000231.1:n.74-4744A=
ENST00000338702.4:c.74-4744A= MANE Select ENSP00000340684.3:n.74-4744A=
NM_000240.3:c.74-4744A= NP_000231.1:n.74-4744A=
NM_001270458.1:c.-326-4744A= NP_001257387.1:n.-326-4744A=
NM_001270458.2:c.-326-4744A= NP_001257387.1:n.-326-4744A=
ENST00000338702.3:c.74-4744A= ENSP00000340684.3:n.74-4744A=
ENST00000497485.1:n.222-4744A=
ENST00000497485.2:n.206-4744A=
ENST00000542639.5:c.-326-4744A= ENSP00000440846.1:n.-326-4744A=
ENST00000542639.6:c.-326-4744A= ENSP00000440846.1:n.-326-4744A=
ENST00000686683.1:c.-537-4744A= ENSP00000509063.1:n.-537-4744A=
ENST00000686980.1:n.206-4744A=
ENST00000688006.1:c.-326-4744A= ENSP00000510311.1:n.-326-4744A=
ENST00000689087.1:c.-326-4744A= ENSP00000508997.1:n.-326-4744A=
ENST00000693128.1:c.74-4744A= ENSP00000508493.1:n.74-4744A=