Canonical Allele Identifier: CA2089294142

Gene: HTR2A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46861205_46861206delinsAG , CM000675.2:g.46861205_46861206delinsAG	GRCh38
NC_000013.10:g.47435340_47435341delinsAG , CM000675.1:g.47435340_47435341delinsAG	GRCh37
NC_000013.9:g.46333341_46333342delinsAG	NCBI36
NG_013011.1:g.40829_40830delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000542664.4:c.614-25567_614-25566delinsCT MANE Select	ENSP00000437737.1:n.614-25567_614-25566de...
ENST00000543956.5:c.125-25567_125-25566delinsCT	ENSP00000441861.2:n.125-25567_125-25566de...
ENST00000378688.8:c.614-25567_614-25566delinsCT	ENSP00000367959.3:n.614-25567_614-25566de...
ENST00000542664.3:c.614-25567_614-25566delinsCT	ENSP00000437737.1:n.614-25567_614-25566de...
ENST00000543956.4:c.362-25567_362-25566delinsCT	ENSP00000441861.1:n.362-25567_362-25566de...
NM_000621.4:c.614-25567_614-25566delinsCT	NP_000612.1:n.614-25567_614-25566delinsCT...
NM_001165947.2:c.362-25567_362-25566delinsCT	NP_001159419.1:n.362-25567_362-25566delin...
NM_000621.5:c.614-25567_614-25566delinsCT MANE Select	NP_000612.1:n.614-25567_614-25566delinsCT...
NM_001165947.5:c.125-25567_125-25566delinsCT	NP_001159419.2:n.125-25567_125-25566delin...
NM_001378924.1:c.614-25567_614-25566delinsCT	NP_001365853.1:n.614-25567_614-25566delin...