Canonical Allele Identifier: CA2622959622
Gene: HTR2A HGNC NCBI

Linked Data

gnomAD v4: 13-46895604-T-TA
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46895605dup , CM000675.2:g.46895605dup GRCh38
NC_000013.10:g.47469740dup , CM000675.1:g.47469740dup GRCh37
NC_000013.9:g.46367741dup NCBI36
NG_013011.1:g.6430dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000542664.4:c.302dup MANE Select ENSP00000437737.1:p.Glu102ArgfsTer19
ENST00000543956.5:c.-78+1069dup ENSP00000441861.2:n.-78+1069dup
ENST00000378688.8:c.302dup ENSP00000367959.3:p.Glu102ArgfsTer19
ENST00000542664.3:c.302dup ENSP00000437737.1:p.Glu102ArgfsTer19
ENST00000543956.4:c.160+1069dup ENSP00000441861.1:n.160+1069dup
ENST00000612998.1:c.209dup ENSP00000482708.1:p.Glu71ArgfsTer19
NM_000621.4:c.302dup NP_000612.1:p.Glu102ArgfsTer19
NM_001165947.2:c.160+1069dup NP_001159419.1:n.160+1069dup
NM_000621.5:c.302dup MANE Select NP_000612.1:p.Glu102ArgfsTer19
NM_001165947.5:c.-78+1069dup NP_001159419.2:n.-78+1069dup
NM_001378924.1:c.302dup NP_001365853.1:p.Glu102ArgfsTer19
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