Canonical Allele Identifier: CA2592686129

Gene: HTR2A

Linked Data

• gnomAD v3: 13-46861309-A-ATTTTTTTT
• gnomAD v4: 13-46861309-A-ATTTTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46861311_46861312insTTTTTTTT , CM000675.2:g.46861311_46861312insTTTTTTTT	GRCh38
NC_000013.10:g.47435446_47435447insTTTTTTTT , CM000675.1:g.47435446_47435447insTTTTTTTT	GRCh37
NC_000013.9:g.46333447_46333448insTTTTTTTT	NCBI36
NG_013011.1:g.40725_40726insAAAAAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.614-25671_614-25670insAAAAAAAA MANE Select	ENSP00000437737.1:n.614-25671_614-25670insAAAAAAAA
ENST00000543956.5:c.125-25671_125-25670insAAAAAAAA	ENSP00000441861.2:n.125-25671_125-25670insAAAAAAAA
ENST00000378688.8:c.614-25671_614-25670insAAAAAAAA	ENSP00000367959.3:n.614-25671_614-25670insAAAAAAAA
ENST00000542664.3:c.614-25671_614-25670insAAAAAAAA	ENSP00000437737.1:n.614-25671_614-25670insAAAAAAAA
ENST00000543956.4:c.362-25671_362-25670insAAAAAAAA	ENSP00000441861.1:n.362-25671_362-25670insAAAAAAAA
NM_000621.4:c.614-25671_614-25670insAAAAAAAA	NP_000612.1:n.614-25671_614-25670insAAAAAAAA
NM_001165947.2:c.362-25671_362-25670insAAAAAAAA	NP_001159419.1:n.362-25671_362-25670insAAAAAAAA
NM_000621.5:c.614-25671_614-25670insAAAAAAAA MANE Select	NP_000612.1:n.614-25671_614-25670insAAAAAAAA
NM_001165947.5:c.125-25671_125-25670insAAAAAAAA	NP_001159419.2:n.125-25671_125-25670insAAAAAAAA
NM_001378924.1:c.614-25671_614-25670insAAAAAAAA	NP_001365853.1:n.614-25671_614-25670insAAAAAAAA