Canonical Allele Identifier: CA2089303225

Gene: HTR2A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46881234_46881235delinsCA , CM000675.2:g.46881234_46881235delinsCA	GRCh38
NC_000013.10:g.47455369_47455370delinsCA , CM000675.1:g.47455369_47455370delinsCA	GRCh37
NC_000013.9:g.46353370_46353371delinsCA	NCBI36
NG_013011.1:g.20800_20801delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.613+11155_613+11156delinsTG MANE Select	ENSP00000437737.1:n.613+11155_613+11156delinsTG
ENST00000543956.5:c.124+11155_124+11156delinsTG	ENSP00000441861.2:n.124+11155_124+11156delinsTG
ENST00000378688.8:c.613+11155_613+11156delinsTG	ENSP00000367959.3:n.613+11155_613+11156delinsTG
ENST00000542664.3:c.613+11155_613+11156delinsTG	ENSP00000437737.1:n.613+11155_613+11156delinsTG
ENST00000543956.4:c.361+11155_361+11156delinsTG	ENSP00000441861.1:n.361+11155_361+11156delinsTG
NM_000621.4:c.613+11155_613+11156delinsTG	NP_000612.1:n.613+11155_613+11156delinsTG
NM_001165947.2:c.361+11155_361+11156delinsTG	NP_001159419.1:n.361+11155_361+11156delinsTG
NM_000621.5:c.613+11155_613+11156delinsTG MANE Select	NP_000612.1:n.613+11155_613+11156delinsTG
NM_001165947.5:c.124+11155_124+11156delinsTG	NP_001159419.2:n.124+11155_124+11156delinsTG
NM_001378924.1:c.613+11155_613+11156delinsTG	NP_001365853.1:n.613+11155_613+11156delinsTG