Canonical Allele Identifier: CA2622959751
Gene: HTR2A HGNC NCBI

Linked Data

gnomAD v4: 13-46896140-ATTAT-A
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46896143_46896146del , CM000675.2:g.46896143_46896146del GRCh38
NC_000013.10:g.47470278_47470281del , CM000675.1:g.47470278_47470281del GRCh37
NC_000013.9:g.46368279_46368282del NCBI36
NG_013011.1:g.5891_5894del

Transcript Alleles

HGVS Amino-acid Change
ENST00000542664.4:c.-238_-235del MANE Select ENSP00000437737.1:n.-238_-235del
ENST00000543956.5:c.-78+530_-78+533del ENSP00000441861.2:n.-78+530_-78+533del
ENST00000542664.3:c.-238_-235del ENSP00000437737.1:n.-238_-235del
ENST00000543956.4:c.160+530_160+533del ENSP00000441861.1:n.160+530_160+533del
NM_000621.4:c.-238_-235del NP_000612.1:n.-238_-235del
NM_001165947.2:c.160+530_160+533del NP_001159419.1:n.160+530_160+533del
NM_000621.5:c.-238_-235del MANE Select NP_000612.1:n.-238_-235del
NM_001165947.5:c.-78+530_-78+533del NP_001159419.2:n.-78+530_-78+533del
NM_001378924.1:c.-238_-235del NP_001365853.1:n.-238_-235del
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