Canonical Allele Identifier: CA2089311367

Gene: HTR2A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46895634_46895635delinsTC , CM000675.2:g.46895634_46895635delinsTC	GRCh38
NC_000013.10:g.47469769_47469770delinsTC , CM000675.1:g.47469769_47469770delinsTC	GRCh37
NC_000013.9:g.46367770_46367771delinsTC	NCBI36
NG_013011.1:g.6400_6401delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.272_273delinsGA MANE Select	ENSP00000437737.1:p.Gly91=
ENST00000543956.5:c.-78+1039_-78+1040delinsGA	ENSP00000441861.2:n.-78+1039_-78+1040delinsGA
ENST00000378688.8:c.272_273delinsGA	ENSP00000367959.3:p.Gly91=
ENST00000542664.3:c.272_273delinsGA	ENSP00000437737.1:p.Gly91=
ENST00000543956.4:c.160+1039_160+1040delinsGA	ENSP00000441861.1:n.160+1039_160+1040delinsGA
ENST00000612998.1:c.179_180delinsGA	ENSP00000482708.1:p.Gly60=
NM_000621.4:c.272_273delinsGA	NP_000612.1:p.Gly91=
NM_001165947.2:c.160+1039_160+1040delinsGA	NP_001159419.1:n.160+1039_160+1040delinsGA
NM_000621.5:c.272_273delinsGA MANE Select	NP_000612.1:p.Gly91=
NM_001165947.5:c.-78+1039_-78+1040delinsGA	NP_001159419.2:n.-78+1039_-78+1040delinsGA
NM_001378924.1:c.272_273delinsGA	NP_001365853.1:p.Gly91=