Canonical Allele Identifier: CA413007606
Gene: MAOA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43731738G>T , CM000685.2:g.43731738G>T GRCh38
NC_000023.10:g.43590985G>T , CM000685.1:g.43590985G>T GRCh37
NC_000023.9:g.43475929G>T NCBI36
NG_008957.2:g.80578G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000542639.6:c.441G>T ENSP00000440846.1:p.Lys147Asn
ENST00000686683.1:c.150G>T ENSP00000509063.1:p.Lys50Asn
ENST00000686980.1:n.972G>T
ENST00000688006.1:c.441G>T ENSP00000510311.1:p.Lys147Asn
ENST00000688859.1:n.396G>T
ENST00000689087.1:c.441G>T ENSP00000508997.1:p.Lys147Asn
ENST00000693128.1:c.735G>T ENSP00000508493.1:p.Lys245Asn
ENST00000338702.4:c.840G>T MANE Select ENSP00000340684.3:p.Lys280Asn
ENST00000338702.3:c.840G>T ENSP00000340684.3:p.Lys280Asn
ENST00000542639.5:c.441G>T ENSP00000440846.1:p.Lys147Asn
NM_000240.3:c.840G>T NP_000231.1:p.Lys280Asn
NM_001270458.1:c.441G>T NP_001257387.1:p.Lys147Asn
NM_000240.4:c.840G>T MANE Select NP_000231.1:p.Lys280Asn
NM_001270458.2:c.441G>T NP_001257387.1:p.Lys147Asn