Canonical Allele Identifier: CA2575412289
Gene: HTR2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46834750del , CM000675.2:g.46834750del GRCh38
NC_000013.10:g.47408885del , CM000675.1:g.47408885del GRCh37
NC_000013.9:g.46306886del NCBI36
NG_013011.1:g.67286del

Transcript Alleles

HGVS Amino-acid change
ENST00000542664.4:c.*88del MANE Select ENSP00000437737.1:n.*88del
ENST00000543956.5:c.*88del ENSP00000441861.2:n.*88del
ENST00000378688.8:c.*88del ENSP00000367959.3:n.*88del
ENST00000542664.3:c.*88del ENSP00000437737.1:n.*88del
ENST00000543956.4:c.*88del ENSP00000441861.1:n.*88del
NM_000621.4:c.*88del NP_000612.1:n.*88del
NM_001165947.2:c.*88del NP_001159419.1:n.*88del
NM_000621.5:c.*88del MANE Select NP_000612.1:n.*88del
NM_001165947.5:c.*88del NP_001159419.2:n.*88del
NM_001378924.1:c.*88del NP_001365853.1:n.*88del