Canonical Allele Identifier: CA2089304424

Gene: HTR2A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46883854_46883856delinsCCA , CM000675.2:g.46883854_46883856delinsCCA	GRCh38
NC_000013.10:g.47457989_47457991delinsCCA , CM000675.1:g.47457989_47457991delinsCCA	GRCh37
NC_000013.9:g.46355990_46355992delinsCCA	NCBI36
NG_013011.1:g.18179_18181delinsTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.613+8534_613+8536delinsTGG MANE Select	ENSP00000437737.1:n.613+8534_613+8536delinsTGG
ENST00000543956.5:c.124+8534_124+8536delinsTGG	ENSP00000441861.2:n.124+8534_124+8536delinsTGG
ENST00000378688.8:c.613+8534_613+8536delinsTGG	ENSP00000367959.3:n.613+8534_613+8536delinsTGG
ENST00000542664.3:c.613+8534_613+8536delinsTGG	ENSP00000437737.1:n.613+8534_613+8536delinsTGG
ENST00000543956.4:c.361+8534_361+8536delinsTGG	ENSP00000441861.1:n.361+8534_361+8536delinsTGG
NM_000621.4:c.613+8534_613+8536delinsTGG	NP_000612.1:n.613+8534_613+8536delinsTGG
NM_001165947.2:c.361+8534_361+8536delinsTGG	NP_001159419.1:n.361+8534_361+8536delinsTGG
NM_000621.5:c.613+8534_613+8536delinsTGG MANE Select	NP_000612.1:n.613+8534_613+8536delinsTGG
NM_001165947.5:c.124+8534_124+8536delinsTGG	NP_001159419.2:n.124+8534_124+8536delinsTGG
NM_001378924.1:c.613+8534_613+8536delinsTGG	NP_001365853.1:n.613+8534_613+8536delinsTGG