Canonical Allele Identifier: CA2089297154

Gene: HTR2A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46867398_46867399delinsAG , CM000675.2:g.46867398_46867399delinsAG	GRCh38
NC_000013.10:g.47441533_47441534delinsAG , CM000675.1:g.47441533_47441534delinsAG	GRCh37
NC_000013.9:g.46339534_46339535delinsAG	NCBI36
NG_013011.1:g.34636_34637delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.613+24991_613+24992delinsCT MANE Select	ENSP00000437737.1:n.613+24991_613+24992delinsCT
ENST00000543956.5:c.124+24991_124+24992delinsCT	ENSP00000441861.2:n.124+24991_124+24992delinsCT
ENST00000378688.8:c.613+24991_613+24992delinsCT	ENSP00000367959.3:n.613+24991_613+24992delinsCT
ENST00000542664.3:c.613+24991_613+24992delinsCT	ENSP00000437737.1:n.613+24991_613+24992delinsCT
ENST00000543956.4:c.361+24991_361+24992delinsCT	ENSP00000441861.1:n.361+24991_361+24992delinsCT
NM_000621.4:c.613+24991_613+24992delinsCT	NP_000612.1:n.613+24991_613+24992delinsCT
NM_001165947.2:c.361+24991_361+24992delinsCT	NP_001159419.1:n.361+24991_361+24992delinsCT
NM_000621.5:c.613+24991_613+24992delinsCT MANE Select	NP_000612.1:n.613+24991_613+24992delinsCT
NM_001165947.5:c.124+24991_124+24992delinsCT	NP_001159419.2:n.124+24991_124+24992delinsCT
NM_001378924.1:c.613+24991_613+24992delinsCT	NP_001365853.1:n.613+24991_613+24992delinsCT