Canonical Allele Identifier: CA2089287696

Gene: HTR2A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46845652_46845661delinsAAAAAAAAAG , CM000675.2:g.46845652_46845661delinsAAAAAAAAAG	GRCh38
NC_000013.10:g.47419787_47419796delinsAAAAAAAAAG , CM000675.1:g.47419787_47419796delinsAAAAAAAAAG	GRCh37
NC_000013.9:g.46317788_46317797delinsAAAAAAAAAG	NCBI36
NG_013011.1:g.56374_56383delinsCTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.614-10022_614-10013delinsCTTTTTTTTT MANE Select	ENSP00000437737.1:n.614-10022_614-10013delinsCTTTTTTTTT
ENST00000543956.5:c.125-10022_125-10013delinsCTTTTTTTTT	ENSP00000441861.2:n.125-10022_125-10013delinsCTTTTTTTTT
ENST00000378688.8:c.614-10022_614-10013delinsCTTTTTTTTT	ENSP00000367959.3:n.614-10022_614-10013delinsCTTTTTTTTT
ENST00000542664.3:c.614-10022_614-10013delinsCTTTTTTTTT	ENSP00000437737.1:n.614-10022_614-10013delinsCTTTTTTTTT
ENST00000543956.4:c.362-10022_362-10013delinsCTTTTTTTTT	ENSP00000441861.1:n.362-10022_362-10013delinsCTTTTTTTTT
NM_000621.4:c.614-10022_614-10013delinsCTTTTTTTTT	NP_000612.1:n.614-10022_614-10013delinsCTTTTTTTTT
NM_001165947.2:c.362-10022_362-10013delinsCTTTTTTTTT	NP_001159419.1:n.362-10022_362-10013delinsCTTTTTTTTT
NM_000621.5:c.614-10022_614-10013delinsCTTTTTTTTT MANE Select	NP_000612.1:n.614-10022_614-10013delinsCTTTTTTTTT
NM_001165947.5:c.125-10022_125-10013delinsCTTTTTTTTT	NP_001159419.2:n.125-10022_125-10013delinsCTTTTTTTTT
NM_001378924.1:c.614-10022_614-10013delinsCTTTTTTTTT	NP_001365853.1:n.614-10022_614-10013delinsCTTTTTTTTT