Canonical Allele Identifier: CA2426669452
Gene: MAOA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43731822G= , CM000685.2:g.43731822G= GRCh38
NC_000023.10:g.43591069G= , CM000685.1:g.43591069G= GRCh37
NC_000023.9:g.43476013G= NCBI36
NG_008957.2:g.80662G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000542639.6:c.525G= ENSP00000440846.1:p.Met175=
ENST00000686683.1:c.234G= ENSP00000509063.1:p.Met78=
ENST00000686980.1:n.1056G=
ENST00000688006.1:c.525G= ENSP00000510311.1:p.Met175=
ENST00000688859.1:n.480G=
ENST00000689087.1:c.525G= ENSP00000508997.1:p.Met175=
ENST00000693128.1:c.819G= ENSP00000508493.1:p.Met273=
ENST00000338702.4:c.924G= MANE Select ENSP00000340684.3:p.Met308=
ENST00000338702.3:c.924G= ENSP00000340684.3:p.Met308=
ENST00000542639.5:c.525G= ENSP00000440846.1:p.Met175=
NM_000240.3:c.924G= NP_000231.1:p.Met308=
NM_001270458.1:c.525G= NP_001257387.1:p.Met175=
NM_000240.4:c.924G= MANE Select NP_000231.1:p.Met308=
NM_001270458.2:c.525G= NP_001257387.1:p.Met175=