Canonical Allele Identifier: CA2089298962

Gene: HTR2A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46871739_46871740delinsTG , CM000675.2:g.46871739_46871740delinsTG	GRCh38
NC_000013.10:g.47445874_47445875delinsTG , CM000675.1:g.47445874_47445875delinsTG	GRCh37
NC_000013.9:g.46343875_46343876delinsTG	NCBI36
NG_013011.1:g.30295_30296delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.613+20650_613+20651delinsCA MANE Select	ENSP00000437737.1:n.613+20650_613+20651delinsCA
ENST00000543956.5:c.124+20650_124+20651delinsCA	ENSP00000441861.2:n.124+20650_124+20651delinsCA
ENST00000378688.8:c.613+20650_613+20651delinsCA	ENSP00000367959.3:n.613+20650_613+20651delinsCA
ENST00000542664.3:c.613+20650_613+20651delinsCA	ENSP00000437737.1:n.613+20650_613+20651delinsCA
ENST00000543956.4:c.361+20650_361+20651delinsCA	ENSP00000441861.1:n.361+20650_361+20651delinsCA
NM_000621.4:c.613+20650_613+20651delinsCA	NP_000612.1:n.613+20650_613+20651delinsCA
NM_001165947.2:c.361+20650_361+20651delinsCA	NP_001159419.1:n.361+20650_361+20651delinsCA
NM_000621.5:c.613+20650_613+20651delinsCA MANE Select	NP_000612.1:n.613+20650_613+20651delinsCA
NM_001165947.5:c.124+20650_124+20651delinsCA	NP_001159419.2:n.124+20650_124+20651delinsCA
NM_001378924.1:c.613+20650_613+20651delinsCA	NP_001365853.1:n.613+20650_613+20651delinsCA