Canonical Allele Identifier: CA249238776
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs201681528

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46861070_46861073del , CM000675.2:g.46861070_46861073del GRCh38
NC_000013.10:g.47435205_47435208del , CM000675.1:g.47435205_47435208del GRCh37
NC_000013.9:g.46333206_46333209del NCBI36
NG_013011.1:g.40964_40967del

Transcript Alleles

HGVS Amino-acid change
ENST00000542664.4:c.614-25432_614-25429del MANE Select ENSP00000437737.1:n.614-25432_614-25429de...
ENST00000543956.5:c.125-25432_125-25429del ENSP00000441861.2:n.125-25432_125-25429de...
ENST00000378688.8:c.614-25432_614-25429del ENSP00000367959.3:n.614-25432_614-25429de...
ENST00000542664.3:c.614-25432_614-25429del ENSP00000437737.1:n.614-25432_614-25429de...
ENST00000543956.4:c.362-25432_362-25429del ENSP00000441861.1:n.362-25432_362-25429de...
NM_000621.4:c.614-25432_614-25429del NP_000612.1:n.614-25432_614-25429del
NM_001165947.2:c.362-25432_362-25429del NP_001159419.1:n.362-25432_362-25429del
NM_000621.5:c.614-25432_614-25429del MANE Select NP_000612.1:n.614-25432_614-25429del
NM_001165947.5:c.125-25432_125-25429del NP_001159419.2:n.125-25432_125-25429del
NM_001378924.1:c.614-25432_614-25429del NP_001365853.1:n.614-25432_614-25429del