Canonical Allele Identifier: CA2994924282

Gene: HTR2A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46837898_46837899insA , CM000675.2:g.46837898_46837899insA	GRCh38
NC_000013.10:g.47412033_47412034insA , CM000675.1:g.47412033_47412034insA	GRCh37
NC_000013.9:g.46310034_46310035insA	NCBI36
NG_013011.1:g.64136_64137insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.614-2260_614-2259insT MANE Select	ENSP00000437737.1:n.614-2260_614-2259insT
ENST00000543956.5:c.125-2260_125-2259insT	ENSP00000441861.2:n.125-2260_125-2259insT
ENST00000378688.8:c.614-2260_614-2259insT	ENSP00000367959.3:n.614-2260_614-2259insT
ENST00000542664.3:c.614-2260_614-2259insT	ENSP00000437737.1:n.614-2260_614-2259insT
ENST00000543956.4:c.362-2260_362-2259insT	ENSP00000441861.1:n.362-2260_362-2259insT
NM_000621.4:c.614-2260_614-2259insT	NP_000612.1:n.614-2260_614-2259insT
NM_001165947.2:c.362-2260_362-2259insT	NP_001159419.1:n.362-2260_362-2259insT
NM_000621.5:c.614-2260_614-2259insT MANE Select	NP_000612.1:n.614-2260_614-2259insT
NM_001165947.5:c.125-2260_125-2259insT	NP_001159419.2:n.125-2260_125-2259insT
NM_001378924.1:c.614-2260_614-2259insT	NP_001365853.1:n.614-2260_614-2259insT