Canonical Allele Identifier: CA2575420758
Gene: HTR2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46895689dup , CM000675.2:g.46895689dup GRCh38
NC_000013.10:g.47469824dup , CM000675.1:g.47469824dup GRCh37
NC_000013.9:g.46367825dup NCBI36
NG_013011.1:g.6352dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000542664.4:c.224dup MANE Select ENSP00000437737.1:p.Asn75LysfsTer?
ENST00000543956.5:c.-78+991dup ENSP00000441861.2:n.-78+991dup
ENST00000378688.8:c.224dup ENSP00000367959.3:p.Asn75LysfsTer?
ENST00000542664.3:c.224dup ENSP00000437737.1:p.Asn75LysfsTer?
ENST00000543956.4:c.160+991dup ENSP00000441861.1:n.160+991dup
ENST00000612998.1:c.131dup ENSP00000482708.1:p.Asn44LysfsTer?
NM_000621.4:c.224dup NP_000612.1:p.Asn75LysfsTer?
NM_001165947.2:c.160+991dup NP_001159419.1:n.160+991dup
NM_000621.5:c.224dup MANE Select NP_000612.1:p.Asn75LysfsTer?
NM_001165947.5:c.-78+991dup NP_001159419.2:n.-78+991dup
NM_001378924.1:c.224dup NP_001365853.1:p.Asn75LysfsTer?