Canonical Allele Identifier: CA2426657736
Gene: MAOA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43693989G= , CM000685.2:g.43693989G= GRCh38
NC_000023.10:g.43553236G= , CM000685.1:g.43553236G= GRCh37
NC_000023.9:g.43438180G= NCBI36
NG_008957.2:g.42829G=

Transcript Alleles

HGVS Amino-acid change
ENST00000497485.2:n.999G=
ENST00000542639.6:c.-94+561G= ENSP00000440846.1:n.-94+561G=
ENST00000686683.1:c.-305+561G= ENSP00000509063.1:n.-305+561G=
ENST00000686980.1:n.438+561G=
ENST00000688006.1:c.-94+561G= ENSP00000510311.1:n.-94+561G=
ENST00000689087.1:c.-94+561G= ENSP00000508997.1:n.-94+561G=
ENST00000693128.1:c.306+561G= ENSP00000508493.1:n.306+561G=
ENST00000338702.4:c.306+561G= MANE Select ENSP00000340684.3:n.306+561G=
ENST00000338702.3:c.306+561G= ENSP00000340684.3:n.306+561G=
ENST00000497485.1:n.454+561G=
ENST00000542639.5:c.-94+561G= ENSP00000440846.1:n.-94+561G=
NM_000240.3:c.306+561G= NP_000231.1:n.306+561G=
NM_001270458.1:c.-94+561G= NP_001257387.1:n.-94+561G=
NM_000240.4:c.306+561G= MANE Select NP_000231.1:n.306+561G=
NM_001270458.2:c.-94+561G= NP_001257387.1:n.-94+561G=