Canonical Allele Identifier: CA249243617

Gene: HTR2A

Linked Data

• dbSNP Id: rs1055759587
• MyVariant Identifiers: chr13:g.47441861_47441862insA (hg19) ; chr13:g.46867726_46867727insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46867726_46867727insA , CM000675.2:g.46867726_46867727insA	GRCh38
NC_000013.10:g.47441861_47441862insA , CM000675.1:g.47441861_47441862insA	GRCh37
NC_000013.9:g.46339862_46339863insA	NCBI36
NG_013011.1:g.34308_34309insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.613+24663_613+24664insT MANE Select	ENSP00000437737.1:n.613+24663_613+24664insT
ENST00000543956.5:c.124+24663_124+24664insT	ENSP00000441861.2:n.124+24663_124+24664insT
ENST00000378688.8:c.613+24663_613+24664insT	ENSP00000367959.3:n.613+24663_613+24664insT
ENST00000542664.3:c.613+24663_613+24664insT	ENSP00000437737.1:n.613+24663_613+24664insT
ENST00000543956.4:c.361+24663_361+24664insT	ENSP00000441861.1:n.361+24663_361+24664insT
NM_000621.4:c.613+24663_613+24664insT	NP_000612.1:n.613+24663_613+24664insT
NM_001165947.2:c.361+24663_361+24664insT	NP_001159419.1:n.361+24663_361+24664insT
NM_000621.5:c.613+24663_613+24664insT MANE Select	NP_000612.1:n.613+24663_613+24664insT
NM_001165947.5:c.124+24663_124+24664insT	NP_001159419.2:n.124+24663_124+24664insT
NM_001378924.1:c.613+24663_613+24664insT	NP_001365853.1:n.613+24663_613+24664insT