Canonical Allele Identifier: CA955698806

Gene: HTR2A

Linked Data

• dbSNP Id: rs1951102602
• gnomAD v3: 13-46896137-TTTA-T
• gnomAD v4: 13-46896137-TTTA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46896143_46896145del , CM000675.2:g.46896143_46896145del	GRCh38
NC_000013.10:g.47470278_47470280del , CM000675.1:g.47470278_47470280del	GRCh37
NC_000013.9:g.46368279_46368281del	NCBI36
NG_013011.1:g.5895_5897del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.-234_-232del MANE Select	ENSP00000437737.1:n.-234_-232del
ENST00000543956.5:c.-78+534_-78+536del	ENSP00000441861.2:n.-78+534_-78+536del
ENST00000542664.3:c.-234_-232del	ENSP00000437737.1:n.-234_-232del
ENST00000543956.4:c.160+534_160+536del	ENSP00000441861.1:n.160+534_160+536del
NM_000621.4:c.-234_-232del	NP_000612.1:n.-234_-232del
NM_001165947.2:c.160+534_160+536del	NP_001159419.1:n.160+534_160+536del
NM_000621.5:c.-234_-232del MANE Select	NP_000612.1:n.-234_-232del
NM_001165947.5:c.-78+534_-78+536del	NP_001159419.2:n.-78+534_-78+536del
NM_001378924.1:c.-234_-232del	NP_001365853.1:n.-234_-232del