Canonical Allele Identifier: CA2089311302

Gene: HTR2A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46895575T= , CM000675.2:g.46895575T=	GRCh38
NC_000013.10:g.47469710T= , CM000675.1:g.47469710T=	GRCh37
NC_000013.9:g.46367711T=	NCBI36
NG_013011.1:g.6460A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.332A= MANE Select	ENSP00000437737.1:p.Tyr111=
ENST00000543956.5:c.-78+1099A=	ENSP00000441861.2:n.-78+1099A=
ENST00000378688.8:c.332A=	ENSP00000367959.3:p.Tyr111=
ENST00000542664.3:c.332A=	ENSP00000437737.1:p.Tyr111=
ENST00000543956.4:c.160+1099A=	ENSP00000441861.1:n.160+1099A=
ENST00000612998.1:c.239A=	ENSP00000482708.1:p.Tyr80=
NM_000621.4:c.332A=	NP_000612.1:p.Tyr111=
NM_001165947.2:c.160+1099A=	NP_001159419.1:n.160+1099A=
NM_000621.5:c.332A= MANE Select	NP_000612.1:p.Tyr111=
NM_001165947.5:c.-78+1099A=	NP_001159419.2:n.-78+1099A=
NM_001378924.1:c.332A=	NP_001365853.1:p.Tyr111=