Canonical Allele Identifier: CA2089311801
Gene: HTR2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46896064_46896068delinsATAGT , CM000675.2:g.46896064_46896068delinsATAGT GRCh38
NC_000013.10:g.47470199_47470203delinsATAGT , CM000675.1:g.47470199_47470203delinsATAGT GRCh37
NC_000013.9:g.46368200_46368204delinsATAGT NCBI36
NG_013011.1:g.5967_5971delinsACTAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000542664.4:c.-162_-158delinsACTAT MANE Select ENSP00000437737.1:n.-162_-158delinsACTAT
ENST00000543956.5:c.-78+606_-78+610delinsACTAT ENSP00000441861.2:n.-78+606_-78+610delinsACTAT
ENST00000542664.3:c.-162_-158delinsACTAT ENSP00000437737.1:n.-162_-158delinsACTAT
ENST00000543956.4:c.160+606_160+610delinsACTAT ENSP00000441861.1:n.160+606_160+610delinsACTAT
NM_000621.4:c.-162_-158delinsACTAT NP_000612.1:n.-162_-158delinsACTAT
NM_001165947.2:c.160+606_160+610delinsACTAT NP_001159419.1:n.160+606_160+610delinsACTAT
NM_000621.5:c.-162_-158delinsACTAT MANE Select NP_000612.1:n.-162_-158delinsACTAT
NM_001165947.5:c.-78+606_-78+610delinsACTAT NP_001159419.2:n.-78+606_-78+610delinsACTAT
NM_001378924.1:c.-162_-158delinsACTAT NP_001365853.1:n.-162_-158delinsACTAT