Canonical Allele Identifier: CA2799080093

Gene: HTR2A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46834769_46834770insAT , CM000675.2:g.46834769_46834770insAT	GRCh38
NC_000013.10:g.47408904_47408905insAT , CM000675.1:g.47408904_47408905insAT	GRCh37
NC_000013.9:g.46306905_46306906insAT	NCBI36
NG_013011.1:g.67266_67267insTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.*68_*69insTA MANE Select	ENSP00000437737.1:n.*68_*69insTA
ENST00000543956.5:c.*68_*69insTA	ENSP00000441861.2:n.*68_*69insTA
ENST00000378688.8:c.*68_*69insTA	ENSP00000367959.3:n.*68_*69insTA
ENST00000542664.3:c.*68_*69insTA	ENSP00000437737.1:n.*68_*69insTA
ENST00000543956.4:c.*68_*69insTA	ENSP00000441861.1:n.*68_*69insTA
NM_000621.4:c.*68_*69insTA	NP_000612.1:n.*68_*69insTA
NM_001165947.2:c.*68_*69insTA	NP_001159419.1:n.*68_*69insTA
NM_000621.5:c.*68_*69insTA MANE Select	NP_000612.1:n.*68_*69insTA
NM_001165947.5:c.*68_*69insTA	NP_001159419.2:n.*68_*69insTA
NM_001378924.1:c.*68_*69insTA	NP_001365853.1:n.*68_*69insTA