Canonical Allele Identifier: CA2089298992
Gene: HTR2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46871808_46871809delinsTC , CM000675.2:g.46871808_46871809delinsTC GRCh38
NC_000013.10:g.47445943_47445944delinsTC , CM000675.1:g.47445943_47445944delinsTC GRCh37
NC_000013.9:g.46343944_46343945delinsTC NCBI36
NG_013011.1:g.30226_30227delinsGA

Transcript Alleles

HGVS Amino-acid change
ENST00000542664.4:c.613+20581_613+20582delinsGA MANE Select ENSP00000437737.1:n.613+20581_613+20582de...
ENST00000543956.5:c.124+20581_124+20582delinsGA ENSP00000441861.2:n.124+20581_124+20582de...
ENST00000378688.8:c.613+20581_613+20582delinsGA ENSP00000367959.3:n.613+20581_613+20582de...
ENST00000542664.3:c.613+20581_613+20582delinsGA ENSP00000437737.1:n.613+20581_613+20582de...
ENST00000543956.4:c.361+20581_361+20582delinsGA ENSP00000441861.1:n.361+20581_361+20582de...
NM_000621.4:c.613+20581_613+20582delinsGA NP_000612.1:n.613+20581_613+20582delinsGA...
NM_001165947.2:c.361+20581_361+20582delinsGA NP_001159419.1:n.361+20581_361+20582delin...
NM_000621.5:c.613+20581_613+20582delinsGA MANE Select NP_000612.1:n.613+20581_613+20582delinsGA...
NM_001165947.5:c.124+20581_124+20582delinsGA NP_001159419.2:n.124+20581_124+20582delin...
NM_001378924.1:c.613+20581_613+20582delinsGA NP_001365853.1:n.613+20581_613+20582delin...