Canonical Allele Identifier: CA955686664

Gene: HTR2A

Linked Data

• gnomAD v3: 13-46834783-A-ATTTTT
• gnomAD v4: 13-46834783-A-ATTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46834784_46834785insTTTTT , CM000675.2:g.46834784_46834785insTTTTT	GRCh38
NC_000013.10:g.47408919_47408920insTTTTT , CM000675.1:g.47408919_47408920insTTTTT	GRCh37
NC_000013.9:g.46306920_46306921insTTTTT	NCBI36
NG_013011.1:g.67251_67252insAAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.*53_*54insAAAAA MANE Select	ENSP00000437737.1:n.*53_*54insAAAAA
ENST00000543956.5:c.*53_*54insAAAAA	ENSP00000441861.2:n.*53_*54insAAAAA
ENST00000378688.8:c.*53_*54insAAAAA	ENSP00000367959.3:n.*53_*54insAAAAA
ENST00000542664.3:c.*53_*54insAAAAA	ENSP00000437737.1:n.*53_*54insAAAAA
ENST00000543956.4:c.*53_*54insAAAAA	ENSP00000441861.1:n.*53_*54insAAAAA
NM_000621.4:c.*53_*54insAAAAA	NP_000612.1:n.*53_*54insAAAAA
NM_001165947.2:c.*53_*54insAAAAA	NP_001159419.1:n.*53_*54insAAAAA
NM_000621.5:c.*53_*54insAAAAA MANE Select	NP_000612.1:n.*53_*54insAAAAA
NM_001165947.5:c.*53_*54insAAAAA	NP_001159419.2:n.*53_*54insAAAAA
NM_001378924.1:c.*53_*54insAAAAA	NP_001365853.1:n.*53_*54insAAAAA