Canonical Allele Identifier: CA2089308841

Gene: HTR2A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46892580C= , CM000675.2:g.46892580C=	GRCh38
NC_000013.10:g.47466715C= , CM000675.1:g.47466715C=	GRCh37
NC_000013.9:g.46364716C=	NCBI36
NG_013011.1:g.9455G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.423G= MANE Select	ENSP00000437737.1:p.Trp141=
ENST00000543956.5:c.-67G=	ENSP00000441861.2:n.-67G=
ENST00000378688.8:c.423G=	ENSP00000367959.3:p.Trp141=
ENST00000542664.3:c.423G=	ENSP00000437737.1:p.Trp141=
ENST00000543956.4:c.171G=	ENSP00000441861.1:p.Trp57=
NM_000621.4:c.423G=	NP_000612.1:p.Trp141=
NM_001165947.2:c.171G=	NP_001159419.1:p.Trp57=
NM_000621.5:c.423G= MANE Select	NP_000612.1:p.Trp141=
NM_001165947.5:c.-67G=	NP_001159419.2:n.-67G=
NM_001378924.1:c.423G=	NP_001365853.1:p.Trp141=