Canonical Allele Identifier: CA2089297148

Gene: HTR2A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46867386_46867387delinsTA , CM000675.2:g.46867386_46867387delinsTA	GRCh38
NC_000013.10:g.47441521_47441522delinsTA , CM000675.1:g.47441521_47441522delinsTA	GRCh37
NC_000013.9:g.46339522_46339523delinsTA	NCBI36
NG_013011.1:g.34648_34649delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.613+25003_613+25004delinsTA MANE Select	ENSP00000437737.1:n.613+25003_613+25004delinsTA
ENST00000543956.5:c.124+25003_124+25004delinsTA	ENSP00000441861.2:n.124+25003_124+25004delinsTA
ENST00000378688.8:c.613+25003_613+25004delinsTA	ENSP00000367959.3:n.613+25003_613+25004delinsTA
ENST00000542664.3:c.613+25003_613+25004delinsTA	ENSP00000437737.1:n.613+25003_613+25004delinsTA
ENST00000543956.4:c.361+25003_361+25004delinsTA	ENSP00000441861.1:n.361+25003_361+25004delinsTA
NM_000621.4:c.613+25003_613+25004delinsTA	NP_000612.1:n.613+25003_613+25004delinsTA
NM_001165947.2:c.361+25003_361+25004delinsTA	NP_001159419.1:n.361+25003_361+25004delinsTA
NM_000621.5:c.613+25003_613+25004delinsTA MANE Select	NP_000612.1:n.613+25003_613+25004delinsTA
NM_001165947.5:c.124+25003_124+25004delinsTA	NP_001159419.2:n.124+25003_124+25004delinsTA
NM_001378924.1:c.613+25003_613+25004delinsTA	NP_001365853.1:n.613+25003_613+25004delinsTA