Canonical Allele Identifier: CA329466082
Community Standard Title: NM_000240.4(MAOA):c.732C>T (p.Val244=)
Gene: MAOA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43731327C>T , CM000685.2:g.43731327C>T GRCh38
NC_000023.10:g.43590574C>T , CM000685.1:g.43590574C>T GRCh37
NC_000023.9:g.43475518C>T NCBI36
NG_008957.2:g.80167C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000240.4:c.732C>T MANE Select NP_000231.1:p.Val244=
ENST00000338702.4:c.732C>T MANE Select ENSP00000340684.3:p.Val244=
NM_000240.3:c.732C>T NP_000231.1:p.Val244=
NM_001270458.1:c.333C>T NP_001257387.1:p.Val111=
NM_001270458.2:c.333C>T NP_001257387.1:p.Val111=
ENST00000338702.3:c.732C>T ENSP00000340684.3:p.Val244=
ENST00000497485.1:n.880C>T
ENST00000542639.5:c.333C>T ENSP00000440846.1:p.Val111=
ENST00000542639.6:c.333C>T ENSP00000440846.1:p.Val111=
ENST00000686683.1:c.42C>T ENSP00000509063.1:p.Val14=
ENST00000686980.1:n.864C>T
ENST00000688006.1:c.333C>T ENSP00000510311.1:p.Val111=
ENST00000688859.1:n.288C>T
ENST00000689087.1:c.333C>T ENSP00000508997.1:p.Val111=
ENST00000693128.1:c.627C>T ENSP00000508493.1:p.Val209=