Canonical Allele Identifier: CA2089293905
Gene: HTR2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46860851_46860853delinsCAG , CM000675.2:g.46860851_46860853delinsCAG GRCh38
NC_000013.10:g.47434986_47434988delinsCAG , CM000675.1:g.47434986_47434988delinsCAG GRCh37
NC_000013.9:g.46332987_46332989delinsCAG NCBI36
NG_013011.1:g.41182_41184delinsCTG

Transcript Alleles

HGVS Amino-acid change
ENST00000542664.4:c.614-25214_614-25212delinsCTG MANE Select ENSP00000437737.1:n.614-25214_614-25212de...
ENST00000543956.5:c.125-25214_125-25212delinsCTG ENSP00000441861.2:n.125-25214_125-25212de...
ENST00000378688.8:c.614-25214_614-25212delinsCTG ENSP00000367959.3:n.614-25214_614-25212de...
ENST00000542664.3:c.614-25214_614-25212delinsCTG ENSP00000437737.1:n.614-25214_614-25212de...
ENST00000543956.4:c.362-25214_362-25212delinsCTG ENSP00000441861.1:n.362-25214_362-25212de...
NM_000621.4:c.614-25214_614-25212delinsCTG NP_000612.1:n.614-25214_614-25212delinsCT...
NM_001165947.2:c.362-25214_362-25212delinsCTG NP_001159419.1:n.362-25214_362-25212delin...
NM_000621.5:c.614-25214_614-25212delinsCTG MANE Select NP_000612.1:n.614-25214_614-25212delinsCT...
NM_001165947.5:c.125-25214_125-25212delinsCTG NP_001159419.2:n.125-25214_125-25212delin...
NM_001378924.1:c.614-25214_614-25212delinsCTG NP_001365853.1:n.614-25214_614-25212delin...