Canonical Allele Identifier: CA2089311698

Gene: HTR2A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46895938_46895941delinsTAGA , CM000675.2:g.46895938_46895941delinsTAGA	GRCh38
NC_000013.10:g.47470073_47470076delinsTAGA , CM000675.1:g.47470073_47470076delinsTAGA	GRCh37
NC_000013.9:g.46368074_46368077delinsTAGA	NCBI36
NG_013011.1:g.6094_6097delinsTCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.-35_-32delinsTCTA MANE Select	ENSP00000437737.1:n.-35_-32delinsTCTA
ENST00000543956.5:c.-78+733_-78+736delinsTCTA	ENSP00000441861.2:n.-78+733_-78+736delinsTCTA
ENST00000378688.8:c.-35_-32delinsTCTA	ENSP00000367959.3:n.-35_-32delinsTCTA
ENST00000542664.3:c.-35_-32delinsTCTA	ENSP00000437737.1:n.-35_-32delinsTCTA
ENST00000543956.4:c.160+733_160+736delinsTCTA	ENSP00000441861.1:n.160+733_160+736delinsTCTA
NM_000621.4:c.-35_-32delinsTCTA	NP_000612.1:n.-35_-32delinsTCTA
NM_001165947.2:c.160+733_160+736delinsTCTA	NP_001159419.1:n.160+733_160+736delinsTCTA
NM_000621.5:c.-35_-32delinsTCTA MANE Select	NP_000612.1:n.-35_-32delinsTCTA
NM_001165947.5:c.-78+733_-78+736delinsTCTA	NP_001159419.2:n.-78+733_-78+736delinsTCTA
NM_001378924.1:c.-35_-32delinsTCTA	NP_001365853.1:n.-35_-32delinsTCTA