Canonical Allele Identifier: CA249254773

Gene: HTR2A

Linked Data

• dbSNP Id: rs939222552
• MyVariant Identifiers: chr13:g.47411805_47411809del (hg19) ; chr13:g.46837670_46837674del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46837675_46837679del , CM000675.2:g.46837675_46837679del	GRCh38
NC_000013.10:g.47411810_47411814del , CM000675.1:g.47411810_47411814del	GRCh37
NC_000013.9:g.46309811_46309815del	NCBI36
NG_013011.1:g.64361_64365del

Transcript Alleles

HGVS	Amino-acid change
ENST00000542664.4:c.614-2035_614-2031del MANE Select	ENSP00000437737.1:n.614-2035_614-2031del
ENST00000543956.5:c.125-2035_125-2031del	ENSP00000441861.2:n.125-2035_125-2031del
ENST00000378688.8:c.614-2035_614-2031del	ENSP00000367959.3:n.614-2035_614-2031del
ENST00000542664.3:c.614-2035_614-2031del	ENSP00000437737.1:n.614-2035_614-2031del
ENST00000543956.4:c.362-2035_362-2031del	ENSP00000441861.1:n.362-2035_362-2031del
NM_000621.4:c.614-2035_614-2031del	NP_000612.1:n.614-2035_614-2031del
NM_001165947.2:c.362-2035_362-2031del	NP_001159419.1:n.362-2035_362-2031del
NM_000621.5:c.614-2035_614-2031del MANE Select	NP_000612.1:n.614-2035_614-2031del
NM_001165947.5:c.125-2035_125-2031del	NP_001159419.2:n.125-2035_125-2031del
NM_001378924.1:c.614-2035_614-2031del	NP_001365853.1:n.614-2035_614-2031del