Canonical Allele Identifier: CA2089311386

Gene: HTR2A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46895669G= , CM000675.2:g.46895669G=	GRCh38
NC_000013.10:g.47469804G= , CM000675.1:g.47469804G=	GRCh37
NC_000013.9:g.46367805G=	NCBI36
NG_013011.1:g.6366C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.238C= MANE Select	ENSP00000437737.1:p.Leu80=
ENST00000543956.5:c.-78+1005C=	ENSP00000441861.2:n.-78+1005C=
ENST00000378688.8:c.238C=	ENSP00000367959.3:p.Leu80=
ENST00000542664.3:c.238C=	ENSP00000437737.1:p.Leu80=
ENST00000543956.4:c.160+1005C=	ENSP00000441861.1:n.160+1005C=
ENST00000612998.1:c.145C=	ENSP00000482708.1:p.Leu49=
NM_000621.4:c.238C=	NP_000612.1:p.Leu80=
NM_001165947.2:c.160+1005C=	NP_001159419.1:n.160+1005C=
NM_000621.5:c.238C= MANE Select	NP_000612.1:p.Leu80=
NM_001165947.5:c.-78+1005C=	NP_001159419.2:n.-78+1005C=
NM_001378924.1:c.238C=	NP_001365853.1:p.Leu80=