Canonical Allele Identifier: CA2089311504
Gene: HTR2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46895788_46895789delinsGA , CM000675.2:g.46895788_46895789delinsGA GRCh38
NC_000013.10:g.47469923_47469924delinsGA , CM000675.1:g.47469923_47469924delinsGA GRCh37
NC_000013.9:g.46367924_46367925delinsGA NCBI36
NG_013011.1:g.6246_6247delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000542664.4:c.118_119delinsTC MANE Select ENSP00000437737.1:p.Ser40=
ENST00000543956.5:c.-78+885_-78+886delinsTC ENSP00000441861.2:n.-78+885_-78+886delinsTC
ENST00000378688.8:c.118_119delinsTC ENSP00000367959.3:p.Ser40=
ENST00000542664.3:c.118_119delinsTC ENSP00000437737.1:p.Ser40=
ENST00000543956.4:c.160+885_160+886delinsTC ENSP00000441861.1:n.160+885_160+886delinsTC
ENST00000612998.1:c.25_26delinsTC ENSP00000482708.1:p.Ser9=
NM_000621.4:c.118_119delinsTC NP_000612.1:p.Ser40=
NM_001165947.2:c.160+885_160+886delinsTC NP_001159419.1:n.160+885_160+886delinsTC
NM_000621.5:c.118_119delinsTC MANE Select NP_000612.1:p.Ser40=
NM_001165947.5:c.-78+885_-78+886delinsTC NP_001159419.2:n.-78+885_-78+886delinsTC
NM_001378924.1:c.118_119delinsTC NP_001365853.1:p.Ser40=