Canonical Allele Identifier: CA955689941

Gene: HTR2A

Linked Data

• gnomAD v3: 13-46845643-C-CAAAAAAAAAAAAAAAAA
• gnomAD v4: 13-46845643-C-CAAAAAAAAAAAAAAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46845644_46845660dup , CM000675.2:g.46845644_46845660dup	GRCh38
NC_000013.10:g.47419779_47419795dup , CM000675.1:g.47419779_47419795dup	GRCh37
NC_000013.9:g.46317780_46317796dup	NCBI36
NG_013011.1:g.56375_56391dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.614-10021_614-10005dup MANE Select	ENSP00000437737.1:n.614-10021_614-10005dup
ENST00000543956.5:c.125-10021_125-10005dup	ENSP00000441861.2:n.125-10021_125-10005dup
ENST00000378688.8:c.614-10021_614-10005dup	ENSP00000367959.3:n.614-10021_614-10005dup
ENST00000542664.3:c.614-10021_614-10005dup	ENSP00000437737.1:n.614-10021_614-10005dup
ENST00000543956.4:c.362-10021_362-10005dup	ENSP00000441861.1:n.362-10021_362-10005dup
NM_000621.4:c.614-10021_614-10005dup	NP_000612.1:n.614-10021_614-10005dup
NM_001165947.2:c.362-10021_362-10005dup	NP_001159419.1:n.362-10021_362-10005dup
NM_000621.5:c.614-10021_614-10005dup MANE Select	NP_000612.1:n.614-10021_614-10005dup
NM_001165947.5:c.125-10021_125-10005dup	NP_001159419.2:n.125-10021_125-10005dup
NM_001378924.1:c.614-10021_614-10005dup	NP_001365853.1:n.614-10021_614-10005dup