Canonical Allele Identifier: CA2622958808
Gene: HTR2A HGNC NCBI

Linked Data

gnomAD v4: 13-46835772-TAA-T
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46835775_46835776del , CM000675.2:g.46835775_46835776del GRCh38
NC_000013.10:g.47409910_47409911del , CM000675.1:g.47409910_47409911del GRCh37
NC_000013.9:g.46307911_46307912del NCBI36
NG_013011.1:g.66261_66262del

Transcript Alleles

HGVS Amino-acid Change
ENST00000542664.4:c.614-135_614-134del MANE Select ENSP00000437737.1:n.614-135_614-134del
ENST00000543956.5:c.125-135_125-134del ENSP00000441861.2:n.125-135_125-134del
ENST00000378688.8:c.614-135_614-134del ENSP00000367959.3:n.614-135_614-134del
ENST00000542664.3:c.614-135_614-134del ENSP00000437737.1:n.614-135_614-134del
ENST00000543956.4:c.362-135_362-134del ENSP00000441861.1:n.362-135_362-134del
NM_000621.4:c.614-135_614-134del NP_000612.1:n.614-135_614-134del
NM_001165947.2:c.362-135_362-134del NP_001159419.1:n.362-135_362-134del
NM_000621.5:c.614-135_614-134del MANE Select NP_000612.1:n.614-135_614-134del
NM_001165947.5:c.125-135_125-134del NP_001159419.2:n.125-135_125-134del
NM_001378924.1:c.614-135_614-134del NP_001365853.1:n.614-135_614-134del
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