Canonical Allele Identifier: CA955689847

Gene: HTR2A

Linked Data

• dbSNP Id: rs11394720
• gnomAD v3: 13-46845643-C-CAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
• gnomAD v4: 13-46845643-C-CAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46845660_46845661insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA , CM000675.2:g.46845660_46845661insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	GRCh38
NC_000013.10:g.47419795_47419796insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA , CM000675.1:g.47419795_47419796insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	GRCh37
NC_000013.9:g.46317796_46317797insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NCBI36
NG_013011.1:g.56391_56392insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.614-10005_614-10004insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select	ENSP00000437737.1:n.614-10005_614-10004insTTTTTTTTTTTTTTTTTTT...
ENST00000543956.5:c.125-10005_125-10004insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000441861.2:n.125-10005_125-10004insTTTTTTTTTTTTTTTTTTT...
ENST00000378688.8:c.614-10005_614-10004insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000367959.3:n.614-10005_614-10004insTTTTTTTTTTTTTTTTTTT...
ENST00000542664.3:c.614-10005_614-10004insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000437737.1:n.614-10005_614-10004insTTTTTTTTTTTTTTTTTTT...
ENST00000543956.4:c.362-10005_362-10004insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000441861.1:n.362-10005_362-10004insTTTTTTTTTTTTTTTTTTT...
NM_000621.4:c.614-10005_614-10004insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NP_000612.1:n.614-10005_614-10004insTTTTTTTTTTTTTTTTTTTTTTTTT...
NM_001165947.2:c.362-10005_362-10004insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NP_001159419.1:n.362-10005_362-10004insTTTTTTTTTTTTTTTTTTTTTT...
NM_000621.5:c.614-10005_614-10004insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select	NP_000612.1:n.614-10005_614-10004insTTTTTTTTTTTTTTTTTTTTTTTTT...
NM_001165947.5:c.125-10005_125-10004insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NP_001159419.2:n.125-10005_125-10004insTTTTTTTTTTTTTTTTTTTTTT...
NM_001378924.1:c.614-10005_614-10004insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NP_001365853.1:n.614-10005_614-10004insTTTTTTTTTTTTTTTTTTTTTT...