Canonical Allele Identifier: CA2592686128
Gene: HTR2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46861302_46861309del , CM000675.2:g.46861302_46861309del GRCh38
NC_000013.10:g.47435437_47435444del , CM000675.1:g.47435437_47435444del GRCh37
NC_000013.9:g.46333438_46333445del NCBI36
NG_013011.1:g.40726_40733del

Transcript Alleles

HGVS Amino-acid Change
ENST00000542664.4:c.614-25670_614-25663del MANE Select ENSP00000437737.1:n.614-25670_614-25663del
ENST00000543956.5:c.125-25670_125-25663del ENSP00000441861.2:n.125-25670_125-25663del
ENST00000378688.8:c.614-25670_614-25663del ENSP00000367959.3:n.614-25670_614-25663del
ENST00000542664.3:c.614-25670_614-25663del ENSP00000437737.1:n.614-25670_614-25663del
ENST00000543956.4:c.362-25670_362-25663del ENSP00000441861.1:n.362-25670_362-25663del
NM_000621.4:c.614-25670_614-25663del NP_000612.1:n.614-25670_614-25663del
NM_001165947.2:c.362-25670_362-25663del NP_001159419.1:n.362-25670_362-25663del
NM_000621.5:c.614-25670_614-25663del MANE Select NP_000612.1:n.614-25670_614-25663del
NM_001165947.5:c.125-25670_125-25663del NP_001159419.2:n.125-25670_125-25663del
NM_001378924.1:c.614-25670_614-25663del NP_001365853.1:n.614-25670_614-25663del