Canonical Allele Identifier: CA955690012

Gene: HTR2A

Linked Data

• gnomAD v3: 13-46845672-T-TAAA
• gnomAD v4: 13-46845672-T-TAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46845673_46845674insAAA , CM000675.2:g.46845673_46845674insAAA	GRCh38
NC_000013.10:g.47419808_47419809insAAA , CM000675.1:g.47419808_47419809insAAA	GRCh37
NC_000013.9:g.46317809_46317810insAAA	NCBI36
NG_013011.1:g.56362_56363insTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.614-10034_614-10033insTTT MANE Select	ENSP00000437737.1:n.614-10034_614-10033insTTT
ENST00000543956.5:c.125-10034_125-10033insTTT	ENSP00000441861.2:n.125-10034_125-10033insTTT
ENST00000378688.8:c.614-10034_614-10033insTTT	ENSP00000367959.3:n.614-10034_614-10033insTTT
ENST00000542664.3:c.614-10034_614-10033insTTT	ENSP00000437737.1:n.614-10034_614-10033insTTT
ENST00000543956.4:c.362-10034_362-10033insTTT	ENSP00000441861.1:n.362-10034_362-10033insTTT
NM_000621.4:c.614-10034_614-10033insTTT	NP_000612.1:n.614-10034_614-10033insTTT
NM_001165947.2:c.362-10034_362-10033insTTT	NP_001159419.1:n.362-10034_362-10033insTTT
NM_000621.5:c.614-10034_614-10033insTTT MANE Select	NP_000612.1:n.614-10034_614-10033insTTT
NM_001165947.5:c.125-10034_125-10033insTTT	NP_001159419.2:n.125-10034_125-10033insTTT
NM_001378924.1:c.614-10034_614-10033insTTT	NP_001365853.1:n.614-10034_614-10033insTTT