Canonical Allele Identifier: CA2089287678
Gene: HTR2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46845638_46845639delinsCA , CM000675.2:g.46845638_46845639delinsCA GRCh38
NC_000013.10:g.47419773_47419774delinsCA , CM000675.1:g.47419773_47419774delinsCA GRCh37
NC_000013.9:g.46317774_46317775delinsCA NCBI36
NG_013011.1:g.56396_56397delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000542664.4:c.614-10000_614-9999delinsTG MANE Select ENSP00000437737.1:n.614-10000_614-9999delinsTG
ENST00000543956.5:c.125-10000_125-9999delinsTG ENSP00000441861.2:n.125-10000_125-9999delinsTG
ENST00000378688.8:c.614-10000_614-9999delinsTG ENSP00000367959.3:n.614-10000_614-9999delinsTG
ENST00000542664.3:c.614-10000_614-9999delinsTG ENSP00000437737.1:n.614-10000_614-9999delinsTG
ENST00000543956.4:c.362-10000_362-9999delinsTG ENSP00000441861.1:n.362-10000_362-9999delinsTG
NM_000621.4:c.614-10000_614-9999delinsTG NP_000612.1:n.614-10000_614-9999delinsTG
NM_001165947.2:c.362-10000_362-9999delinsTG NP_001159419.1:n.362-10000_362-9999delinsTG
NM_000621.5:c.614-10000_614-9999delinsTG MANE Select NP_000612.1:n.614-10000_614-9999delinsTG
NM_001165947.5:c.125-10000_125-9999delinsTG NP_001159419.2:n.125-10000_125-9999delinsTG
NM_001378924.1:c.614-10000_614-9999delinsTG NP_001365853.1:n.614-10000_614-9999delinsTG