Canonical Allele Identifier: CA2622959683
Gene: HTR2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46896024_46896037del , CM000675.2:g.46896024_46896037del GRCh38
NC_000013.10:g.47470159_47470172del , CM000675.1:g.47470159_47470172del GRCh37
NC_000013.9:g.46368160_46368173del NCBI36
NG_013011.1:g.6002_6015del

Transcript Alleles

HGVS Amino-acid Change
ENST00000542664.4:c.-127_-114del MANE Select ENSP00000437737.1:n.-127_-114del
ENST00000543956.5:c.-78+641_-78+654del ENSP00000441861.2:n.-78+641_-78+654del
ENST00000378688.8:c.-127_-114del ENSP00000367959.3:n.-127_-114del
ENST00000542664.3:c.-127_-114del ENSP00000437737.1:n.-127_-114del
ENST00000543956.4:c.160+641_160+654del ENSP00000441861.1:n.160+641_160+654del
NM_000621.4:c.-127_-114del NP_000612.1:n.-127_-114del
NM_001165947.2:c.160+641_160+654del NP_001159419.1:n.160+641_160+654del
NM_000621.5:c.-127_-114del MANE Select NP_000612.1:n.-127_-114del
NM_001165947.5:c.-78+641_-78+654del NP_001159419.2:n.-78+641_-78+654del
NM_001378924.1:c.-127_-114del NP_001365853.1:n.-127_-114del