Canonical Allele Identifier: CA2089304362

Gene: HTR2A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46883706_46883708delinsTCA , CM000675.2:g.46883706_46883708delinsTCA	GRCh38
NC_000013.10:g.47457841_47457843delinsTCA , CM000675.1:g.47457841_47457843delinsTCA	GRCh37
NC_000013.9:g.46355842_46355844delinsTCA	NCBI36
NG_013011.1:g.18327_18329delinsTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.613+8682_613+8684delinsTGA MANE Select	ENSP00000437737.1:n.613+8682_613+8684delinsTGA
ENST00000543956.5:c.124+8682_124+8684delinsTGA	ENSP00000441861.2:n.124+8682_124+8684delinsTGA
ENST00000378688.8:c.613+8682_613+8684delinsTGA	ENSP00000367959.3:n.613+8682_613+8684delinsTGA
ENST00000542664.3:c.613+8682_613+8684delinsTGA	ENSP00000437737.1:n.613+8682_613+8684delinsTGA
ENST00000543956.4:c.361+8682_361+8684delinsTGA	ENSP00000441861.1:n.361+8682_361+8684delinsTGA
NM_000621.4:c.613+8682_613+8684delinsTGA	NP_000612.1:n.613+8682_613+8684delinsTGA
NM_001165947.2:c.361+8682_361+8684delinsTGA	NP_001159419.1:n.361+8682_361+8684delinsTGA
NM_000621.5:c.613+8682_613+8684delinsTGA MANE Select	NP_000612.1:n.613+8682_613+8684delinsTGA
NM_001165947.5:c.124+8682_124+8684delinsTGA	NP_001159419.2:n.124+8682_124+8684delinsTGA
NM_001378924.1:c.613+8682_613+8684delinsTGA	NP_001365853.1:n.613+8682_613+8684delinsTGA