Canonical Allele Identifier: CA2089292790

Gene: HTR2A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46859253_46859256delinsCATT , CM000675.2:g.46859253_46859256delinsCATT	GRCh38
NC_000013.10:g.47433388_47433391delinsCATT , CM000675.1:g.47433388_47433391delinsCATT	GRCh37
NC_000013.9:g.46331389_46331392delinsCATT	NCBI36
NG_013011.1:g.42779_42782delinsAATG

Transcript Alleles

HGVS	Amino-acid change
ENST00000542664.4:c.614-23617_614-23614delinsAATG MANE Select	ENSP00000437737.1:n.614-23617_614-23614de...
ENST00000543956.5:c.125-23617_125-23614delinsAATG	ENSP00000441861.2:n.125-23617_125-23614de...
ENST00000378688.8:c.614-23617_614-23614delinsAATG	ENSP00000367959.3:n.614-23617_614-23614de...
ENST00000542664.3:c.614-23617_614-23614delinsAATG	ENSP00000437737.1:n.614-23617_614-23614de...
ENST00000543956.4:c.362-23617_362-23614delinsAATG	ENSP00000441861.1:n.362-23617_362-23614de...
NM_000621.4:c.614-23617_614-23614delinsAATG	NP_000612.1:n.614-23617_614-23614delinsAA...
NM_001165947.2:c.362-23617_362-23614delinsAATG	NP_001159419.1:n.362-23617_362-23614delin...
NM_000621.5:c.614-23617_614-23614delinsAATG MANE Select	NP_000612.1:n.614-23617_614-23614delinsAA...
NM_001165947.5:c.125-23617_125-23614delinsAATG	NP_001159419.2:n.125-23617_125-23614delin...
NM_001378924.1:c.614-23617_614-23614delinsAATG	NP_001365853.1:n.614-23617_614-23614delin...