Canonical Allele Identifier: CA2089284399
Gene: HTR2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46837654_46837655delinsAG , CM000675.2:g.46837654_46837655delinsAG GRCh38
NC_000013.10:g.47411789_47411790delinsAG , CM000675.1:g.47411789_47411790delinsAG GRCh37
NC_000013.9:g.46309790_46309791delinsAG NCBI36
NG_013011.1:g.64380_64381delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000542664.4:c.614-2016_614-2015delinsCT MANE Select ENSP00000437737.1:n.614-2016_614-2015delinsCT
ENST00000543956.5:c.125-2016_125-2015delinsCT ENSP00000441861.2:n.125-2016_125-2015delinsCT
ENST00000378688.8:c.614-2016_614-2015delinsCT ENSP00000367959.3:n.614-2016_614-2015delinsCT
ENST00000542664.3:c.614-2016_614-2015delinsCT ENSP00000437737.1:n.614-2016_614-2015delinsCT
ENST00000543956.4:c.362-2016_362-2015delinsCT ENSP00000441861.1:n.362-2016_362-2015delinsCT
NM_000621.4:c.614-2016_614-2015delinsCT NP_000612.1:n.614-2016_614-2015delinsCT
NM_001165947.2:c.362-2016_362-2015delinsCT NP_001159419.1:n.362-2016_362-2015delinsCT
NM_000621.5:c.614-2016_614-2015delinsCT MANE Select NP_000612.1:n.614-2016_614-2015delinsCT
NM_001165947.5:c.125-2016_125-2015delinsCT NP_001159419.2:n.125-2016_125-2015delinsCT
NM_001378924.1:c.614-2016_614-2015delinsCT NP_001365853.1:n.614-2016_614-2015delinsCT