Canonical Allele Identifier: CA2089283635

Gene: HTR2A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46835714_46835715delinsAT , CM000675.2:g.46835714_46835715delinsAT	GRCh38
NC_000013.10:g.47409849_47409850delinsAT , CM000675.1:g.47409849_47409850delinsAT	GRCh37
NC_000013.9:g.46307850_46307851delinsAT	NCBI36
NG_013011.1:g.66320_66321delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.614-76_614-75delinsAT MANE Select	ENSP00000437737.1:n.614-76_614-75delinsAT
ENST00000543956.5:c.125-76_125-75delinsAT	ENSP00000441861.2:n.125-76_125-75delinsAT
ENST00000378688.8:c.614-76_614-75delinsAT	ENSP00000367959.3:n.614-76_614-75delinsAT
ENST00000542664.3:c.614-76_614-75delinsAT	ENSP00000437737.1:n.614-76_614-75delinsAT
ENST00000543956.4:c.362-76_362-75delinsAT	ENSP00000441861.1:n.362-76_362-75delinsAT
NM_000621.4:c.614-76_614-75delinsAT	NP_000612.1:n.614-76_614-75delinsAT
NM_001165947.2:c.362-76_362-75delinsAT	NP_001159419.1:n.362-76_362-75delinsAT
NM_000621.5:c.614-76_614-75delinsAT MANE Select	NP_000612.1:n.614-76_614-75delinsAT
NM_001165947.5:c.125-76_125-75delinsAT	NP_001159419.2:n.125-76_125-75delinsAT
NM_001378924.1:c.614-76_614-75delinsAT	NP_001365853.1:n.614-76_614-75delinsAT