Canonical Allele Identifier: CA2622959622

Gene: HTR2A

Linked Data

• gnomAD v4: 13-46895604-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46895605dup , CM000675.2:g.46895605dup	GRCh38
NC_000013.10:g.47469740dup , CM000675.1:g.47469740dup	GRCh37
NC_000013.9:g.46367741dup	NCBI36
NG_013011.1:g.6430dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.302dup MANE Select	ENSP00000437737.1:p.Glu102ArgfsTer19
ENST00000543956.5:c.-78+1069dup	ENSP00000441861.2:n.-78+1069dup
ENST00000378688.8:c.302dup	ENSP00000367959.3:p.Glu102ArgfsTer19
ENST00000542664.3:c.302dup	ENSP00000437737.1:p.Glu102ArgfsTer19
ENST00000543956.4:c.160+1069dup	ENSP00000441861.1:n.160+1069dup
ENST00000612998.1:c.209dup	ENSP00000482708.1:p.Glu71ArgfsTer19
NM_000621.4:c.302dup	NP_000612.1:p.Glu102ArgfsTer19
NM_001165947.2:c.160+1069dup	NP_001159419.1:n.160+1069dup
NM_000621.5:c.302dup MANE Select	NP_000612.1:p.Glu102ArgfsTer19
NM_001165947.5:c.-78+1069dup	NP_001159419.2:n.-78+1069dup
NM_001378924.1:c.302dup	NP_001365853.1:p.Glu102ArgfsTer19