Canonical Allele Identifier: CA2089294162
Gene: HTR2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46861227_46861231delinsAATTC , CM000675.2:g.46861227_46861231delinsAATTC GRCh38
NC_000013.10:g.47435362_47435366delinsAATTC , CM000675.1:g.47435362_47435366delinsAATTC GRCh37
NC_000013.9:g.46333363_46333367delinsAATTC NCBI36
NG_013011.1:g.40804_40808delinsGAATT

Transcript Alleles

HGVS Amino-acid change
ENST00000542664.4:c.614-25592_614-25588delinsGAATT MANE Select ENSP00000437737.1:n.614-25592_614-25588de...
ENST00000543956.5:c.125-25592_125-25588delinsGAATT ENSP00000441861.2:n.125-25592_125-25588de...
ENST00000378688.8:c.614-25592_614-25588delinsGAATT ENSP00000367959.3:n.614-25592_614-25588de...
ENST00000542664.3:c.614-25592_614-25588delinsGAATT ENSP00000437737.1:n.614-25592_614-25588de...
ENST00000543956.4:c.362-25592_362-25588delinsGAATT ENSP00000441861.1:n.362-25592_362-25588de...
NM_000621.4:c.614-25592_614-25588delinsGAATT NP_000612.1:n.614-25592_614-25588delinsGA...
NM_001165947.2:c.362-25592_362-25588delinsGAATT NP_001159419.1:n.362-25592_362-25588delin...
NM_000621.5:c.614-25592_614-25588delinsGAATT MANE Select NP_000612.1:n.614-25592_614-25588delinsGA...
NM_001165947.5:c.125-25592_125-25588delinsGAATT NP_001159419.2:n.125-25592_125-25588delin...
NM_001378924.1:c.614-25592_614-25588delinsGAATT NP_001365853.1:n.614-25592_614-25588delin...