Canonical Allele Identifier: CA2505138417

Gene: HTR2A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46866204_46866205insGATAAAGATAG , CM000675.2:g.46866204_46866205insGATAAAGATAG	GRCh38
NC_000013.10:g.47440339_47440340insGATAAAGATAG , CM000675.1:g.47440339_47440340insGATAAAGATAG	GRCh37
NC_000013.9:g.46338340_46338341insGATAAAGATAG	NCBI36
NG_013011.1:g.35830_35831insCTATCTTTATC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.613+26185_613+26186insCTATCTTTATC MANE Select	ENSP00000437737.1:n.613+26185_613+26186insCTATCTTTATC
ENST00000543956.5:c.124+26185_124+26186insCTATCTTTATC	ENSP00000441861.2:n.124+26185_124+26186insCTATCTTTATC
ENST00000378688.8:c.613+26185_613+26186insCTATCTTTATC	ENSP00000367959.3:n.613+26185_613+26186insCTATCTTTATC
ENST00000542664.3:c.613+26185_613+26186insCTATCTTTATC	ENSP00000437737.1:n.613+26185_613+26186insCTATCTTTATC
ENST00000543956.4:c.361+26185_361+26186insCTATCTTTATC	ENSP00000441861.1:n.361+26185_361+26186insCTATCTTTATC
NM_000621.4:c.613+26185_613+26186insCTATCTTTATC	NP_000612.1:n.613+26185_613+26186insCTATCTTTATC
NM_001165947.2:c.361+26185_361+26186insCTATCTTTATC	NP_001159419.1:n.361+26185_361+26186insCTATCTTTATC
NM_000621.5:c.613+26185_613+26186insCTATCTTTATC MANE Select	NP_000612.1:n.613+26185_613+26186insCTATCTTTATC
NM_001165947.5:c.124+26185_124+26186insCTATCTTTATC	NP_001159419.2:n.124+26185_124+26186insCTATCTTTATC
NM_001378924.1:c.613+26185_613+26186insCTATCTTTATC	NP_001365853.1:n.613+26185_613+26186insCTATCTTTATC