Canonical Allele Identifier: CA2543633925
Gene: HTR2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46883962_46883963insTCATCGTGTCTGGACCAGCCGTTTCAAAAGGTTATATGAATAATCCAGAGAAAACA , CM000675.2:g.46883962_46883963insTCATCGTGTCTGGACCAGCCGTTTCAAAAGGTTATATGAATAATCCAGAGAAAACA GRCh38
NC_000013.10:g.47458097_47458098insTCATCGTGTCTGGACCAGCCGTTTCAAAAGGTTATATGAATAATCCAGAGAAAACA , CM000675.1:g.47458097_47458098insTCATCGTGTCTGGACCAGCCGTTTCAAAAGGTTATATGAATAATCCAGAGAAAACA GRCh37
NC_000013.9:g.46356098_46356099insTCATCGTGTCTGGACCAGCCGTTTCAAAAGGTTATATGAATAATCCAGAGAAAACA NCBI36
NG_013011.1:g.18073_18074insGTTTTCTCTGGATTATTCATATAACCTTTTGAAACGGCTGGTCCAGACACGATGAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000542664.4:c.613+8428_613+8429insGTTTTCTCTGGATTATTCATATAACCTTTTGAAACGGCTGGTCCAGACACGATGAT MANE Select ENSP00000437737.1:n.613+8428_613+8429insGTTTTCTCTGGATTATTCATA...
ENST00000543956.5:c.124+8428_124+8429insGTTTTCTCTGGATTATTCATATAACCTTTTGAAACGGCTGGTCCAGACACGATGAT ENSP00000441861.2:n.124+8428_124+8429insGTTTTCTCTGGATTATTCATA...
ENST00000378688.8:c.613+8428_613+8429insGTTTTCTCTGGATTATTCATATAACCTTTTGAAACGGCTGGTCCAGACACGATGAT ENSP00000367959.3:n.613+8428_613+8429insGTTTTCTCTGGATTATTCATA...
ENST00000542664.3:c.613+8428_613+8429insGTTTTCTCTGGATTATTCATATAACCTTTTGAAACGGCTGGTCCAGACACGATGAT ENSP00000437737.1:n.613+8428_613+8429insGTTTTCTCTGGATTATTCATA...
ENST00000543956.4:c.361+8428_361+8429insGTTTTCTCTGGATTATTCATATAACCTTTTGAAACGGCTGGTCCAGACACGATGAT ENSP00000441861.1:n.361+8428_361+8429insGTTTTCTCTGGATTATTCATA...
NM_000621.4:c.613+8428_613+8429insGTTTTCTCTGGATTATTCATATAACCTTTTGAAACGGCTGGTCCAGACACGATGAT NP_000612.1:n.613+8428_613+8429insGTTTTCTCTGGATTATTCATATAACCT...
NM_001165947.2:c.361+8428_361+8429insGTTTTCTCTGGATTATTCATATAACCTTTTGAAACGGCTGGTCCAGACACGATGAT NP_001159419.1:n.361+8428_361+8429insGTTTTCTCTGGATTATTCATATAA...
NM_000621.5:c.613+8428_613+8429insGTTTTCTCTGGATTATTCATATAACCTTTTGAAACGGCTGGTCCAGACACGATGAT MANE Select NP_000612.1:n.613+8428_613+8429insGTTTTCTCTGGATTATTCATATAACCT...
NM_001165947.5:c.124+8428_124+8429insGTTTTCTCTGGATTATTCATATAACCTTTTGAAACGGCTGGTCCAGACACGATGAT NP_001159419.2:n.124+8428_124+8429insGTTTTCTCTGGATTATTCATATAA...
NM_001378924.1:c.613+8428_613+8429insGTTTTCTCTGGATTATTCATATAACCTTTTGAAACGGCTGGTCCAGACACGATGAT NP_001365853.1:n.613+8428_613+8429insGTTTTCTCTGGATTATTCATATAA...