Canonical Allele Identifier: CA2840814978

Gene: HTR2A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46871774_46871780del , CM000675.2:g.46871774_46871780del	GRCh38
NC_000013.10:g.47445909_47445915del , CM000675.1:g.47445909_47445915del	GRCh37
NC_000013.9:g.46343910_46343916del	NCBI36
NG_013011.1:g.30256_30262del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.613+20611_613+20617del MANE Select	ENSP00000437737.1:n.613+20611_613+20617del
ENST00000543956.5:c.124+20611_124+20617del	ENSP00000441861.2:n.124+20611_124+20617del
ENST00000378688.8:c.613+20611_613+20617del	ENSP00000367959.3:n.613+20611_613+20617del
ENST00000542664.3:c.613+20611_613+20617del	ENSP00000437737.1:n.613+20611_613+20617del
ENST00000543956.4:c.361+20611_361+20617del	ENSP00000441861.1:n.361+20611_361+20617del
NM_000621.4:c.613+20611_613+20617del	NP_000612.1:n.613+20611_613+20617del
NM_001165947.2:c.361+20611_361+20617del	NP_001159419.1:n.361+20611_361+20617del
NM_000621.5:c.613+20611_613+20617del MANE Select	NP_000612.1:n.613+20611_613+20617del
NM_001165947.5:c.124+20611_124+20617del	NP_001159419.2:n.124+20611_124+20617del
NM_001378924.1:c.613+20611_613+20617del	NP_001365853.1:n.613+20611_613+20617del