Canonical Allele Identifier: CA2622959724

Gene: HTR2A

Linked Data

• gnomAD v4: 13-46896082-TGTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46896087_46896089del , CM000675.2:g.46896087_46896089del	GRCh38
NC_000013.10:g.47470222_47470224del , CM000675.1:g.47470222_47470224del	GRCh37
NC_000013.9:g.46368223_46368225del	NCBI36
NG_013011.1:g.5950_5952del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.-179_-177del MANE Select	ENSP00000437737.1:n.-179_-177del
ENST00000543956.5:c.-78+589_-78+591del	ENSP00000441861.2:n.-78+589_-78+591del
ENST00000542664.3:c.-179_-177del	ENSP00000437737.1:n.-179_-177del
ENST00000543956.4:c.160+589_160+591del	ENSP00000441861.1:n.160+589_160+591del
NM_000621.4:c.-179_-177del	NP_000612.1:n.-179_-177del
NM_001165947.2:c.160+589_160+591del	NP_001159419.1:n.160+589_160+591del
NM_000621.5:c.-179_-177del MANE Select	NP_000612.1:n.-179_-177del
NM_001165947.5:c.-78+589_-78+591del	NP_001159419.2:n.-78+589_-78+591del
NM_001378924.1:c.-179_-177del	NP_001365853.1:n.-179_-177del