Canonical Allele Identifier: CA2089292853

Gene: HTR2A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46859357_46859358delinsTC , CM000675.2:g.46859357_46859358delinsTC	GRCh38
NC_000013.10:g.47433492_47433493delinsTC , CM000675.1:g.47433492_47433493delinsTC	GRCh37
NC_000013.9:g.46331493_46331494delinsTC	NCBI36
NG_013011.1:g.42677_42678delinsGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000542664.4:c.614-23719_614-23718delinsGA MANE Select	ENSP00000437737.1:n.614-23719_614-23718delinsGA
ENST00000543956.5:c.125-23719_125-23718delinsGA	ENSP00000441861.2:n.125-23719_125-23718delinsGA
ENST00000378688.8:c.614-23719_614-23718delinsGA	ENSP00000367959.3:n.614-23719_614-23718delinsGA
ENST00000542664.3:c.614-23719_614-23718delinsGA	ENSP00000437737.1:n.614-23719_614-23718delinsGA
ENST00000543956.4:c.362-23719_362-23718delinsGA	ENSP00000441861.1:n.362-23719_362-23718delinsGA
NM_000621.4:c.614-23719_614-23718delinsGA	NP_000612.1:n.614-23719_614-23718delinsGA
NM_001165947.2:c.362-23719_362-23718delinsGA	NP_001159419.1:n.362-23719_362-23718delinsGA
NM_000621.5:c.614-23719_614-23718delinsGA MANE Select	NP_000612.1:n.614-23719_614-23718delinsGA
NM_001165947.5:c.125-23719_125-23718delinsGA	NP_001159419.2:n.125-23719_125-23718delinsGA
NM_001378924.1:c.614-23719_614-23718delinsGA	NP_001365853.1:n.614-23719_614-23718delinsGA