Canonical Allele Identifier: CA2089283388
Gene: HTR2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46834963_46834964delinsCT , CM000675.2:g.46834963_46834964delinsCT GRCh38
NC_000013.10:g.47409098_47409099delinsCT , CM000675.1:g.47409098_47409099delinsCT GRCh37
NC_000013.9:g.46307099_46307100delinsCT NCBI36
NG_013011.1:g.67071_67072delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000542664.4:c.1289_1290delinsAG MANE Select ENSP00000437737.1:p.Lys430=
ENST00000543956.5:c.800_801delinsAG ENSP00000441861.2:p.Lys267=
ENST00000378688.8:c.1289_1290delinsAG ENSP00000367959.3:p.Lys430=
ENST00000542664.3:c.1289_1290delinsAG ENSP00000437737.1:p.Lys430=
ENST00000543956.4:c.1037_1038delinsAG ENSP00000441861.1:p.Lys346=
NM_000621.4:c.1289_1290delinsAG NP_000612.1:p.Lys430=
NM_001165947.2:c.1037_1038delinsAG NP_001159419.1:p.Lys346=
NM_000621.5:c.1289_1290delinsAG MANE Select NP_000612.1:p.Lys430=
NM_001165947.5:c.800_801delinsAG NP_001159419.2:p.Lys267=
NM_001378924.1:c.1289_1290delinsAG NP_001365853.1:p.Lys430=