Canonical Allele Identifier: CA2089283382

Gene: HTR2A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46834950C= , CM000675.2:g.46834950C=	GRCh38
NC_000013.10:g.47409085C= , CM000675.1:g.47409085C=	GRCh37
NC_000013.9:g.46307086C=	NCBI36
NG_013011.1:g.67085G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.1303G= MANE Select	ENSP00000437737.1:p.Asp435=
ENST00000543956.5:c.814G=	ENSP00000441861.2:p.Asp272=
ENST00000378688.8:c.1303G=	ENSP00000367959.3:p.Asp435=
ENST00000542664.3:c.1303G=	ENSP00000437737.1:p.Asp435=
ENST00000543956.4:c.1051G=	ENSP00000441861.1:p.Asp351=
NM_000621.4:c.1303G=	NP_000612.1:p.Asp435=
NM_001165947.2:c.1051G=	NP_001159419.1:p.Asp351=
NM_000621.5:c.1303G= MANE Select	NP_000612.1:p.Asp435=
NM_001165947.5:c.814G=	NP_001159419.2:p.Asp272=
NM_001378924.1:c.1303G=	NP_001365853.1:p.Asp435=