Canonical Allele Identifier: CA2426674026
Community Standard Title: NM_000240.4(MAOA):c.*1081A=
Gene: MAOA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43745594A= , CM000685.2:g.43745594A= GRCh38
NC_000023.10:g.43604841A= , CM000685.1:g.43604841A= GRCh37
NC_000023.9:g.43489785A= NCBI36
NG_008957.2:g.94434A=

Transcript Alleles

HGVS Amino-acid Change
NM_000240.4:c.*1081A= MANE Select NP_000231.1:n.*1081A=
ENST00000338702.4:c.*1081A= MANE Select ENSP00000340684.3:n.*1081A=
NM_000240.3:c.*1081A= NP_000231.1:n.*1081A=
NM_001270458.1:c.*1081A= NP_001257387.1:n.*1081A=
NM_001270458.2:c.*1081A= NP_001257387.1:n.*1081A=
ENST00000338702.3:c.*1081A= ENSP00000340684.3:n.*1081A=
ENST00000542639.5:c.*1081A= ENSP00000440846.1:n.*1081A=
ENST00000542639.6:c.*1081A= ENSP00000440846.1:n.*1081A=
ENST00000686683.1:c.*1081A= ENSP00000509063.1:n.*1081A=
ENST00000686980.1:n.7197A=
ENST00000688006.1:c.*1081A= ENSP00000510311.1:n.*1081A=
ENST00000689087.1:c.*1081A= ENSP00000508997.1:n.*1081A=
ENST00000693128.1:c.*1081A= ENSP00000508493.1:n.*1081A=