Canonical Allele Identifier: CA2089292794

Gene: HTR2A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46859260_46859261delinsCA , CM000675.2:g.46859260_46859261delinsCA	GRCh38
NC_000013.10:g.47433395_47433396delinsCA , CM000675.1:g.47433395_47433396delinsCA	GRCh37
NC_000013.9:g.46331396_46331397delinsCA	NCBI36
NG_013011.1:g.42774_42775delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000542664.4:c.614-23622_614-23621delinsTG MANE Select	ENSP00000437737.1:n.614-23622_614-23621de...
ENST00000543956.5:c.125-23622_125-23621delinsTG	ENSP00000441861.2:n.125-23622_125-23621de...
ENST00000378688.8:c.614-23622_614-23621delinsTG	ENSP00000367959.3:n.614-23622_614-23621de...
ENST00000542664.3:c.614-23622_614-23621delinsTG	ENSP00000437737.1:n.614-23622_614-23621de...
ENST00000543956.4:c.362-23622_362-23621delinsTG	ENSP00000441861.1:n.362-23622_362-23621de...
NM_000621.4:c.614-23622_614-23621delinsTG	NP_000612.1:n.614-23622_614-23621delinsTG...
NM_001165947.2:c.362-23622_362-23621delinsTG	NP_001159419.1:n.362-23622_362-23621delin...
NM_000621.5:c.614-23622_614-23621delinsTG MANE Select	NP_000612.1:n.614-23622_614-23621delinsTG...
NM_001165947.5:c.125-23622_125-23621delinsTG	NP_001159419.2:n.125-23622_125-23621delin...
NM_001378924.1:c.614-23622_614-23621delinsTG	NP_001365853.1:n.614-23622_614-23621delin...