Canonical Allele Identifier: CA2089311335

Gene: HTR2A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46895608_46895610delinsGAC , CM000675.2:g.46895608_46895610delinsGAC	GRCh38
NC_000013.10:g.47469743_47469745delinsGAC , CM000675.1:g.47469743_47469745delinsGAC	GRCh37
NC_000013.9:g.46367744_46367746delinsGAC	NCBI36
NG_013011.1:g.6425_6427delinsGTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.297_299delinsGTC MANE Select	ENSP00000437737.1:p.Val99=
ENST00000543956.5:c.-78+1064_-78+1066delinsGTC	ENSP00000441861.2:n.-78+1064_-78+1066delinsGTC
ENST00000378688.8:c.297_299delinsGTC	ENSP00000367959.3:p.Val99=
ENST00000542664.3:c.297_299delinsGTC	ENSP00000437737.1:p.Val99=
ENST00000543956.4:c.160+1064_160+1066delinsGTC	ENSP00000441861.1:n.160+1064_160+1066delinsGTC
ENST00000612998.1:c.204_206delinsGTC	ENSP00000482708.1:p.Val68=
NM_000621.4:c.297_299delinsGTC	NP_000612.1:p.Val99=
NM_001165947.2:c.160+1064_160+1066delinsGTC	NP_001159419.1:n.160+1064_160+1066delinsGTC
NM_000621.5:c.297_299delinsGTC MANE Select	NP_000612.1:p.Val99=
NM_001165947.5:c.-78+1064_-78+1066delinsGTC	NP_001159419.2:n.-78+1064_-78+1066delinsGTC
NM_001378924.1:c.297_299delinsGTC	NP_001365853.1:p.Val99=