Canonical Allele Identifier: CA698562922

Gene: HTR2A

Linked Data

• dbSNP Id: rs1356387737
• MyVariant Identifiers: chr13:g.47423660_47423663del (hg19) ; chr13:g.46849525_46849528del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46849529_46849532del , CM000675.2:g.46849529_46849532del	GRCh38
NC_000013.10:g.47423664_47423667del , CM000675.1:g.47423664_47423667del	GRCh37
NC_000013.9:g.46321665_46321668del	NCBI36
NG_013011.1:g.52507_52510del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.614-13889_614-13886del MANE Select	ENSP00000437737.1:n.614-13889_614-13886del
ENST00000543956.5:c.125-13889_125-13886del	ENSP00000441861.2:n.125-13889_125-13886del
ENST00000378688.8:c.614-13889_614-13886del	ENSP00000367959.3:n.614-13889_614-13886del
ENST00000542664.3:c.614-13889_614-13886del	ENSP00000437737.1:n.614-13889_614-13886del
ENST00000543956.4:c.362-13889_362-13886del	ENSP00000441861.1:n.362-13889_362-13886del
NM_000621.4:c.614-13889_614-13886del	NP_000612.1:n.614-13889_614-13886del
NM_001165947.2:c.362-13889_362-13886del	NP_001159419.1:n.362-13889_362-13886del
NM_000621.5:c.614-13889_614-13886del MANE Select	NP_000612.1:n.614-13889_614-13886del
NM_001165947.5:c.125-13889_125-13886del	NP_001159419.2:n.125-13889_125-13886del
NM_001378924.1:c.614-13889_614-13886del	NP_001365853.1:n.614-13889_614-13886del