Canonical Allele Identifier: CA2622958700

Gene: HTR2A

Linked Data

• gnomAD v4: 13-46834778-T-TTTC

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46834778_46834779insTTC , CM000675.2:g.46834778_46834779insTTC	GRCh38
NC_000013.10:g.47408913_47408914insTTC , CM000675.1:g.47408913_47408914insTTC	GRCh37
NC_000013.9:g.46306914_46306915insTTC	NCBI36
NG_013011.1:g.67256_67257insGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.*58_*59insGAA MANE Select	ENSP00000437737.1:n.*58_*59insGAA
ENST00000543956.5:c.*58_*59insGAA	ENSP00000441861.2:n.*58_*59insGAA
ENST00000378688.8:c.*58_*59insGAA	ENSP00000367959.3:n.*58_*59insGAA
ENST00000542664.3:c.*58_*59insGAA	ENSP00000437737.1:n.*58_*59insGAA
ENST00000543956.4:c.*58_*59insGAA	ENSP00000441861.1:n.*58_*59insGAA
NM_000621.4:c.*58_*59insGAA	NP_000612.1:n.*58_*59insGAA
NM_001165947.2:c.*58_*59insGAA	NP_001159419.1:n.*58_*59insGAA
NM_000621.5:c.*58_*59insGAA MANE Select	NP_000612.1:n.*58_*59insGAA
NM_001165947.5:c.*58_*59insGAA	NP_001159419.2:n.*58_*59insGAA
NM_001378924.1:c.*58_*59insGAA	NP_001365853.1:n.*58_*59insGAA