Canonical Allele Identifier: CA698569547

Gene: HTR2A

Linked Data

• dbSNP Id: rs1201960058
• MyVariant Identifiers: chr13:g.47435437_47435438insCTAAAAAT (hg19) ; chr13:g.46861302_46861303insCTAAAAAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46861303_46861310dup , CM000675.2:g.46861303_46861310dup	GRCh38
NC_000013.10:g.47435438_47435445dup , CM000675.1:g.47435438_47435445dup	GRCh37
NC_000013.9:g.46333439_46333446dup	NCBI36
NG_013011.1:g.40725_40732dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.614-25671_614-25664dup MANE Select	ENSP00000437737.1:n.614-25671_614-25664dup
ENST00000543956.5:c.125-25671_125-25664dup	ENSP00000441861.2:n.125-25671_125-25664dup
ENST00000378688.8:c.614-25671_614-25664dup	ENSP00000367959.3:n.614-25671_614-25664dup
ENST00000542664.3:c.614-25671_614-25664dup	ENSP00000437737.1:n.614-25671_614-25664dup
ENST00000543956.4:c.362-25671_362-25664dup	ENSP00000441861.1:n.362-25671_362-25664dup
NM_000621.4:c.614-25671_614-25664dup	NP_000612.1:n.614-25671_614-25664dup
NM_001165947.2:c.362-25671_362-25664dup	NP_001159419.1:n.362-25671_362-25664dup
NM_000621.5:c.614-25671_614-25664dup MANE Select	NP_000612.1:n.614-25671_614-25664dup
NM_001165947.5:c.125-25671_125-25664dup	NP_001159419.2:n.125-25671_125-25664dup
NM_001378924.1:c.614-25671_614-25664dup	NP_001365853.1:n.614-25671_614-25664dup