Canonical Allele Identifier: CA2622958752

Gene: HTR2A

Linked Data

• gnomAD v4: 13-46834963-C-CT

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.1289dup MANE Select	ENSP00000437737.1:p.Asn431GlufsTer11
ENST00000543956.5:c.800dup	ENSP00000441861.2:p.Asn268GlufsTer11
ENST00000378688.8:c.1289dup	ENSP00000367959.3:p.Asn431GlufsTer11
ENST00000542664.3:c.1289dup	ENSP00000437737.1:p.Asn431GlufsTer11
ENST00000543956.4:c.1037dup	ENSP00000441861.1:p.Asn347GlufsTer11
NM_000621.4:c.1289dup	NP_000612.1:p.Asn431GlufsTer11
NM_001165947.2:c.1037dup	NP_001159419.1:p.Asn347GlufsTer11
NM_000621.5:c.1289dup MANE Select	NP_000612.1:p.Asn431GlufsTer11
NM_001165947.5:c.800dup	NP_001159419.2:p.Asn268GlufsTer11
NM_001378924.1:c.1289dup	NP_001365853.1:p.Asn431GlufsTer11