Canonical Allele Identifier: CA609929162

Gene: HTR2A

Linked Data

• dbSNP Id: rs1398128295
• gnomAD v2: 13-47409098-CT-C
• gnomAD v4: 13-46834963-CT-C
• MyVariant Identifiers: chr13:g.47409099del (hg19) ; chr13:g.46834964del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46834970del , CM000675.2:g.46834970del	GRCh38
NC_000013.10:g.47409105del , CM000675.1:g.47409105del	GRCh37
NC_000013.9:g.46307106del	NCBI36
NG_013011.1:g.67071del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.1289del MANE Select	ENSP00000437737.1:p.Lys430ArgfsTer19
ENST00000543956.5:c.800del	ENSP00000441861.2:p.Lys267ArgfsTer19
ENST00000378688.8:c.1289del	ENSP00000367959.3:p.Lys430ArgfsTer19
ENST00000542664.3:c.1289del	ENSP00000437737.1:p.Lys430ArgfsTer19
ENST00000543956.4:c.1037del	ENSP00000441861.1:p.Lys346ArgfsTer19
NM_000621.4:c.1289del	NP_000612.1:p.Lys430ArgfsTer19
NM_001165947.2:c.1037del	NP_001159419.1:p.Lys346ArgfsTer19
NM_000621.5:c.1289del MANE Select	NP_000612.1:p.Lys430ArgfsTer19
NM_001165947.5:c.800del	NP_001159419.2:p.Lys267ArgfsTer19
NM_001378924.1:c.1289del	NP_001365853.1:p.Lys430ArgfsTer19