Canonical Allele Identifier: CA2510882890

Gene: HTR2A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46837728_46837729insTGCGGATAAACAGAATGAGATACGTGATAAGTTGTATAAGGACATCAACACGTGGCTTAGTAATCGAGACAATAGCGGTCAGTCTCTTCTTGCCTTCACCTTTATGGGTACTGATGGTAAAGA , CM000675.2:g.46837728_46837729insTGCGGATAAACAGAATGAGATACGTGATAAGTTGTATAAGGACATCAACACGTGGCTTAGTAATCGAGACAATAGCGGTCAGTCTCTTCTTGCCTTCACCTTTATGGGTACTGATGGTAAAGA	GRCh38
NC_000013.10:g.47411863_47411864insTGCGGATAAACAGAATGAGATACGTGATAAGTTGTATAAGGACATCAACACGTGGCTTAGTAATCGAGACAATAGCGGTCAGTCTCTTCTTGCCTTCACCTTTATGGGTACTGATGGTAAAGA , CM000675.1:g.47411863_47411864insTGCGGATAAACAGAATGAGATACGTGATAAGTTGTATAAGGACATCAACACGTGGCTTAGTAATCGAGACAATAGCGGTCAGTCTCTTCTTGCCTTCACCTTTATGGGTACTGATGGTAAAGA	GRCh37
NC_000013.9:g.46309864_46309865insTGCGGATAAACAGAATGAGATACGTGATAAGTTGTATAAGGACATCAACACGTGGCTTAGTAATCGAGACAATAGCGGTCAGTCTCTTCTTGCCTTCACCTTTATGGGTACTGATGGTAAAGA	NCBI36
NG_013011.1:g.64308_64309insTTTACCATCAGTACCCATAAAGGTGAAGGCAAGAAGAGACTGACCGCTATTGTCTCGATTACTAAGCCACGTGTTGATGTCCTTATACAACTTATCACGTATCTCATTCTGTTTATCCGCATC

Transcript Alleles

HGVS	Amino-acid change
ENST00000542664.4:c.614-2088_614-2087insTTTACCATCAGTACCCATAAAGGTGAAGGCAAGAAGAGACTGACCGCTATTGTCTCGATTACTAAGCCACGTGTTGATGTCCTTATACAACTTATCACGTATCTCATTCTGTTTATCCGCATC MANE Select	ENSP00000437737.1:n.614-2088_614-2087insT...
ENST00000543956.5:c.125-2088_125-2087insTTTACCATCAGTACCCATAAAGGTGAAGGCAAGAAGAGACTGACCGCTATTGTCTCGATTACTAAGCCACGTGTTGATGTCCTTATACAACTTATCACGTATCTCATTCTGTTTATCCGCATC	ENSP00000441861.2:n.125-2088_125-2087insT...
ENST00000378688.8:c.614-2088_614-2087insTTTACCATCAGTACCCATAAAGGTGAAGGCAAGAAGAGACTGACCGCTATTGTCTCGATTACTAAGCCACGTGTTGATGTCCTTATACAACTTATCACGTATCTCATTCTGTTTATCCGCATC	ENSP00000367959.3:n.614-2088_614-2087insT...
ENST00000542664.3:c.614-2088_614-2087insTTTACCATCAGTACCCATAAAGGTGAAGGCAAGAAGAGACTGACCGCTATTGTCTCGATTACTAAGCCACGTGTTGATGTCCTTATACAACTTATCACGTATCTCATTCTGTTTATCCGCATC	ENSP00000437737.1:n.614-2088_614-2087insT...
ENST00000543956.4:c.362-2088_362-2087insTTTACCATCAGTACCCATAAAGGTGAAGGCAAGAAGAGACTGACCGCTATTGTCTCGATTACTAAGCCACGTGTTGATGTCCTTATACAACTTATCACGTATCTCATTCTGTTTATCCGCATC	ENSP00000441861.1:n.362-2088_362-2087insT...
NM_000621.4:c.614-2088_614-2087insTTTACCATCAGTACCCATAAAGGTGAAGGCAAGAAGAGACTGACCGCTATTGTCTCGATTACTAAGCCACGTGTTGATGTCCTTATACAACTTATCACGTATCTCATTCTGTTTATCCGCATC	NP_000612.1:n.614-2088_614-2087insTTTACCA...
NM_001165947.2:c.362-2088_362-2087insTTTACCATCAGTACCCATAAAGGTGAAGGCAAGAAGAGACTGACCGCTATTGTCTCGATTACTAAGCCACGTGTTGATGTCCTTATACAACTTATCACGTATCTCATTCTGTTTATCCGCATC	NP_001159419.1:n.362-2088_362-2087insTTTA...
NM_000621.5:c.614-2088_614-2087insTTTACCATCAGTACCCATAAAGGTGAAGGCAAGAAGAGACTGACCGCTATTGTCTCGATTACTAAGCCACGTGTTGATGTCCTTATACAACTTATCACGTATCTCATTCTGTTTATCCGCATC MANE Select	NP_000612.1:n.614-2088_614-2087insTTTACCA...
NM_001165947.5:c.125-2088_125-2087insTTTACCATCAGTACCCATAAAGGTGAAGGCAAGAAGAGACTGACCGCTATTGTCTCGATTACTAAGCCACGTGTTGATGTCCTTATACAACTTATCACGTATCTCATTCTGTTTATCCGCATC	NP_001159419.2:n.125-2088_125-2087insTTTA...
NM_001378924.1:c.614-2088_614-2087insTTTACCATCAGTACCCATAAAGGTGAAGGCAAGAAGAGACTGACCGCTATTGTCTCGATTACTAAGCCACGTGTTGATGTCCTTATACAACTTATCACGTATCTCATTCTGTTTATCCGCATC	NP_001365853.1:n.614-2088_614-2087insTTTA...