Canonical Allele Identifier: CA2592685883
Gene: HTR2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46835804dup , CM000675.2:g.46835804dup GRCh38
NC_000013.10:g.47409939dup , CM000675.1:g.47409939dup GRCh37
NC_000013.9:g.46307940dup NCBI36
NG_013011.1:g.66231dup

Transcript Alleles

HGVS Amino-acid change
ENST00000542664.4:c.614-165dup MANE Select ENSP00000437737.1:n.614-165dup
ENST00000543956.5:c.125-165dup ENSP00000441861.2:n.125-165dup
ENST00000378688.8:c.614-165dup ENSP00000367959.3:n.614-165dup
ENST00000542664.3:c.614-165dup ENSP00000437737.1:n.614-165dup
ENST00000543956.4:c.362-165dup ENSP00000441861.1:n.362-165dup
NM_000621.4:c.614-165dup NP_000612.1:n.614-165dup
NM_001165947.2:c.362-165dup NP_001159419.1:n.362-165dup
NM_000621.5:c.614-165dup MANE Select NP_000612.1:n.614-165dup
NM_001165947.5:c.125-165dup NP_001159419.2:n.125-165dup
NM_001378924.1:c.614-165dup NP_001365853.1:n.614-165dup