Canonical Allele Identifier: CA2089311732

Gene: HTR2A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46895975C= , CM000675.2:g.46895975C=	GRCh38
NC_000013.10:g.47470110C= , CM000675.1:g.47470110C=	GRCh37
NC_000013.9:g.46368111C=	NCBI36
NG_013011.1:g.6060G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.-69G= MANE Select	ENSP00000437737.1:n.-69G=
ENST00000543956.5:c.-78+699G=	ENSP00000441861.2:n.-78+699G=
ENST00000378688.8:c.-69G=	ENSP00000367959.3:n.-69G=
ENST00000542664.3:c.-69G=	ENSP00000437737.1:n.-69G=
ENST00000543956.4:c.160+699G=	ENSP00000441861.1:n.160+699G=
NM_000621.4:c.-69G=	NP_000612.1:n.-69G=
NM_001165947.2:c.160+699G=	NP_001159419.1:n.160+699G=
NM_000621.5:c.-69G= MANE Select	NP_000612.1:n.-69G=
NM_001165947.5:c.-78+699G=	NP_001159419.2:n.-78+699G=
NM_001378924.1:c.-69G=	NP_001365853.1:n.-69G=