Canonical Allele Identifier: CA2089304430

Gene: HTR2A

Linked Data

• dbSNP Id: rs1950985823

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46883866_46883870del , CM000675.2:g.46883866_46883870del	GRCh38
NC_000013.10:g.47458001_47458005del , CM000675.1:g.47458001_47458005del	GRCh37
NC_000013.9:g.46356002_46356006del	NCBI36
NG_013011.1:g.18167_18171del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.613+8522_613+8526del MANE Select	ENSP00000437737.1:n.613+8522_613+8526del
ENST00000543956.5:c.124+8522_124+8526del	ENSP00000441861.2:n.124+8522_124+8526del
ENST00000378688.8:c.613+8522_613+8526del	ENSP00000367959.3:n.613+8522_613+8526del
ENST00000542664.3:c.613+8522_613+8526del	ENSP00000437737.1:n.613+8522_613+8526del
ENST00000543956.4:c.361+8522_361+8526del	ENSP00000441861.1:n.361+8522_361+8526del
NM_000621.4:c.613+8522_613+8526del	NP_000612.1:n.613+8522_613+8526del
NM_001165947.2:c.361+8522_361+8526del	NP_001159419.1:n.361+8522_361+8526del
NM_000621.5:c.613+8522_613+8526del MANE Select	NP_000612.1:n.613+8522_613+8526del
NM_001165947.5:c.124+8522_124+8526del	NP_001159419.2:n.124+8522_124+8526del
NM_001378924.1:c.613+8522_613+8526del	NP_001365853.1:n.613+8522_613+8526del