Canonical Allele Identifier: CA698569322

Gene: HTR2A

Linked Data

• dbSNP Id: rs1443821143
• MyVariant Identifiers: chr13:g.47434924_47434934del (hg19) ; chr13:g.46860789_46860799del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46860789_46860799del , CM000675.2:g.46860789_46860799del	GRCh38
NC_000013.10:g.47434924_47434934del , CM000675.1:g.47434924_47434934del	GRCh37
NC_000013.9:g.46332925_46332935del	NCBI36
NG_013011.1:g.41236_41246del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.614-25160_614-25150del MANE Select	ENSP00000437737.1:n.614-25160_614-25150del
ENST00000543956.5:c.125-25160_125-25150del	ENSP00000441861.2:n.125-25160_125-25150del
ENST00000378688.8:c.614-25160_614-25150del	ENSP00000367959.3:n.614-25160_614-25150del
ENST00000542664.3:c.614-25160_614-25150del	ENSP00000437737.1:n.614-25160_614-25150del
ENST00000543956.4:c.362-25160_362-25150del	ENSP00000441861.1:n.362-25160_362-25150del
NM_000621.4:c.614-25160_614-25150del	NP_000612.1:n.614-25160_614-25150del
NM_001165947.2:c.362-25160_362-25150del	NP_001159419.1:n.362-25160_362-25150del
NM_000621.5:c.614-25160_614-25150del MANE Select	NP_000612.1:n.614-25160_614-25150del
NM_001165947.5:c.125-25160_125-25150del	NP_001159419.2:n.125-25160_125-25150del
NM_001378924.1:c.614-25160_614-25150del	NP_001365853.1:n.614-25160_614-25150del