Canonical Allele Identifier: CA2089308851

Gene: HTR2A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46892587T= , CM000675.2:g.46892587T=	GRCh38
NC_000013.10:g.47466722T= , CM000675.1:g.47466722T=	GRCh37
NC_000013.9:g.46364723T=	NCBI36
NG_013011.1:g.9448A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.416A= MANE Select	ENSP00000437737.1:p.Tyr139=
ENST00000543956.5:c.-74A=	ENSP00000441861.2:n.-74A=
ENST00000378688.8:c.416A=	ENSP00000367959.3:p.Tyr139=
ENST00000542664.3:c.416A=	ENSP00000437737.1:p.Tyr139=
ENST00000543956.4:c.164A=	ENSP00000441861.1:p.Tyr55=
NM_000621.4:c.416A=	NP_000612.1:p.Tyr139=
NM_001165947.2:c.164A=	NP_001159419.1:p.Tyr55=
NM_000621.5:c.416A= MANE Select	NP_000612.1:p.Tyr139=
NM_001165947.5:c.-74A=	NP_001159419.2:n.-74A=
NM_001378924.1:c.416A=	NP_001365853.1:p.Tyr139=