Canonical Allele Identifier: CA2089284345

Gene: HTR2A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46837526_46837528delinsCAA , CM000675.2:g.46837526_46837528delinsCAA	GRCh38
NC_000013.10:g.47411661_47411663delinsCAA , CM000675.1:g.47411661_47411663delinsCAA	GRCh37
NC_000013.9:g.46309662_46309664delinsCAA	NCBI36
NG_013011.1:g.64507_64509delinsTTG

Transcript Alleles

HGVS	Amino-acid Change
NM_000621.5:c.614-1889_614-1887delinsTTG MANE Select	NP_000612.1:n.614-1889_614-1887delinsTTG
ENST00000542664.4:c.614-1889_614-1887delinsTTG MANE Select	ENSP00000437737.1:n.614-1889_614-1887delinsTTG
NM_000621.4:c.614-1889_614-1887delinsTTG	NP_000612.1:n.614-1889_614-1887delinsTTG
NM_001165947.2:c.362-1889_362-1887delinsTTG	NP_001159419.1:n.362-1889_362-1887delinsTTG
NM_001165947.5:c.125-1889_125-1887delinsTTG	NP_001159419.2:n.125-1889_125-1887delinsTTG
NM_001378924.1:c.614-1889_614-1887delinsTTG	NP_001365853.1:n.614-1889_614-1887delinsTTG
ENST00000378688.8:c.614-1889_614-1887delinsTTG	ENSP00000367959.3:n.614-1889_614-1887delinsTTG
ENST00000542664.3:c.614-1889_614-1887delinsTTG	ENSP00000437737.1:n.614-1889_614-1887delinsTTG
ENST00000543956.4:c.362-1889_362-1887delinsTTG	ENSP00000441861.1:n.362-1889_362-1887delinsTTG
ENST00000543956.5:c.125-1889_125-1887delinsTTG	ENSP00000441861.2:n.125-1889_125-1887delinsTTG