Canonical Allele Identifier: CA2622959623

Gene: HTR2A

Linked Data

• gnomAD v4: 13-46895641-ATAGT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46895645_46895648del , CM000675.2:g.46895645_46895648del	GRCh38
NC_000013.10:g.47469780_47469783del , CM000675.1:g.47469780_47469783del	GRCh37
NC_000013.9:g.46367781_46367784del	NCBI36
NG_013011.1:g.6390_6393del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.262_265del MANE Select	ENSP00000437737.1:p.Thr88LeufsTer13
ENST00000543956.5:c.-78+1029_-78+1032del	ENSP00000441861.2:n.-78+1029_-78+1032del
ENST00000378688.8:c.262_265del	ENSP00000367959.3:p.Thr88LeufsTer13
ENST00000542664.3:c.262_265del	ENSP00000437737.1:p.Thr88LeufsTer13
ENST00000543956.4:c.160+1029_160+1032del	ENSP00000441861.1:n.160+1029_160+1032del
ENST00000612998.1:c.169_172del	ENSP00000482708.1:p.Thr57LeufsTer13
NM_000621.4:c.262_265del	NP_000612.1:p.Thr88LeufsTer13
NM_001165947.2:c.160+1029_160+1032del	NP_001159419.1:n.160+1029_160+1032del
NM_000621.5:c.262_265del MANE Select	NP_000612.1:p.Thr88LeufsTer13
NM_001165947.5:c.-78+1029_-78+1032del	NP_001159419.2:n.-78+1029_-78+1032del
NM_001378924.1:c.262_265del	NP_001365853.1:p.Thr88LeufsTer13