Canonical Allele Identifier: CA2622959722

Gene: HTR2A

Linked Data

• gnomAD v4: 13-46896077-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46896077_46896078insC , CM000675.2:g.46896077_46896078insC	GRCh38
NC_000013.10:g.47470212_47470213insC , CM000675.1:g.47470212_47470213insC	GRCh37
NC_000013.9:g.46368213_46368214insC	NCBI36
NG_013011.1:g.5957_5958insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.-172_-171insG MANE Select	ENSP00000437737.1:n.-172_-171insG
ENST00000543956.5:c.-78+596_-78+597insG	ENSP00000441861.2:n.-78+596_-78+597insG
ENST00000542664.3:c.-172_-171insG	ENSP00000437737.1:n.-172_-171insG
ENST00000543956.4:c.160+596_160+597insG	ENSP00000441861.1:n.160+596_160+597insG
NM_000621.4:c.-172_-171insG	NP_000612.1:n.-172_-171insG
NM_001165947.2:c.160+596_160+597insG	NP_001159419.1:n.160+596_160+597insG
NM_000621.5:c.-172_-171insG MANE Select	NP_000612.1:n.-172_-171insG
NM_001165947.5:c.-78+596_-78+597insG	NP_001159419.2:n.-78+596_-78+597insG
NM_001378924.1:c.-172_-171insG	NP_001365853.1:n.-172_-171insG