Canonical Allele Identifier: CA2566490367

Gene: HTR2A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46837725_46837726insCAGAG , CM000675.2:g.46837725_46837726insCAGAG	GRCh38
NC_000013.10:g.47411860_47411861insCAGAG , CM000675.1:g.47411860_47411861insCAGAG	GRCh37
NC_000013.9:g.46309861_46309862insCAGAG	NCBI36
NG_013011.1:g.64309_64310insCTCTG

Transcript Alleles

HGVS	Amino-acid Change
NM_000621.5:c.614-2087_614-2086insCTCTG MANE Select	NP_000612.1:n.614-2087_614-2086insCTCTG
ENST00000542664.4:c.614-2087_614-2086insCTCTG MANE Select	ENSP00000437737.1:n.614-2087_614-2086insCTCTG
NM_000621.4:c.614-2087_614-2086insCTCTG	NP_000612.1:n.614-2087_614-2086insCTCTG
NM_001165947.2:c.362-2087_362-2086insCTCTG	NP_001159419.1:n.362-2087_362-2086insCTCTG
NM_001165947.5:c.125-2087_125-2086insCTCTG	NP_001159419.2:n.125-2087_125-2086insCTCTG
NM_001378924.1:c.614-2087_614-2086insCTCTG	NP_001365853.1:n.614-2087_614-2086insCTCTG
ENST00000378688.8:c.614-2087_614-2086insCTCTG	ENSP00000367959.3:n.614-2087_614-2086insCTCTG
ENST00000542664.3:c.614-2087_614-2086insCTCTG	ENSP00000437737.1:n.614-2087_614-2086insCTCTG
ENST00000543956.4:c.362-2087_362-2086insCTCTG	ENSP00000441861.1:n.362-2087_362-2086insCTCTG
ENST00000543956.5:c.125-2087_125-2086insCTCTG	ENSP00000441861.2:n.125-2087_125-2086insCTCTG