Canonical Allele Identifier: CA698543741

Gene: HTR2A

Linked Data

• dbSNP Id: rs1453552222
• MyVariant Identifiers: chr13:g.47466997_47466998del (hg19) ; chr13:g.46892862_46892863del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46892865_46892866del , CM000675.2:g.46892865_46892866del	GRCh38
NC_000013.10:g.47467000_47467001del , CM000675.1:g.47467000_47467001del	GRCh37
NC_000013.9:g.46365001_46365002del	NCBI36
NG_013011.1:g.9172_9173del

Transcript Alleles

HGVS	Amino-acid change
ENST00000542664.4:c.413-273_413-272del MANE Select	ENSP00000437737.1:n.413-273_413-272del
ENST00000543956.5:c.-77-273_-77-272del	ENSP00000441861.2:n.-77-273_-77-272del
ENST00000378688.8:c.413-273_413-272del	ENSP00000367959.3:n.413-273_413-272del
ENST00000542664.3:c.413-273_413-272del	ENSP00000437737.1:n.413-273_413-272del
ENST00000543956.4:c.161-273_161-272del	ENSP00000441861.1:n.161-273_161-272del
NM_000621.4:c.413-273_413-272del	NP_000612.1:n.413-273_413-272del
NM_001165947.2:c.161-273_161-272del	NP_001159419.1:n.161-273_161-272del
NM_000621.5:c.413-273_413-272del MANE Select	NP_000612.1:n.413-273_413-272del
NM_001165947.5:c.-77-273_-77-272del	NP_001159419.2:n.-77-273_-77-272del
NM_001378924.1:c.413-273_413-272del	NP_001365853.1:n.413-273_413-272del