Canonical Allele Identifier: CA2622958750
Gene: HTR2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46834885_46834886insCTAAA , CM000675.2:g.46834885_46834886insCTAAA GRCh38
NC_000013.10:g.47409020_47409021insCTAAA , CM000675.1:g.47409020_47409021insCTAAA GRCh37
NC_000013.9:g.46307021_46307022insCTAAA NCBI36
NG_013011.1:g.67151_67152insTAGTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000542664.4:c.1369_1370insTAGTT MANE Select ENSP00000437737.1:p.Ser457LeufsTer10
ENST00000543956.5:c.880_881insTAGTT ENSP00000441861.2:p.Ser294LeufsTer10
ENST00000378688.8:c.1369_1370insTAGTT ENSP00000367959.3:p.Ser457LeufsTer10
ENST00000542664.3:c.1369_1370insTAGTT ENSP00000437737.1:p.Ser457LeufsTer10
ENST00000543956.4:c.1117_1118insTAGTT ENSP00000441861.1:p.Ser373LeufsTer10
NM_000621.4:c.1369_1370insTAGTT NP_000612.1:p.Ser457LeufsTer10
NM_001165947.2:c.1117_1118insTAGTT NP_001159419.1:p.Ser373LeufsTer10
NM_000621.5:c.1369_1370insTAGTT MANE Select NP_000612.1:p.Ser457LeufsTer10
NM_001165947.5:c.880_881insTAGTT NP_001159419.2:p.Ser294LeufsTer10
NM_001378924.1:c.1369_1370insTAGTT NP_001365853.1:p.Ser457LeufsTer10