Canonical Allele Identifier: CA891835229

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960961_87960962delinsCT , CM000672.2:g.87960961_87960962delinsCT	GRCh38
NC_000010.10:g.89720718_89720719delinsCT , CM000672.1:g.89720718_89720719delinsCT	GRCh37
NC_000010.9:g.89710698_89710699delinsCT	NCBI36
NG_007466.2:g.102523_102524delinsCT , LRG_311:g.102523_102524delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.962_963delinsCT	ENSP00000514759.2:p.Val321Ala
ENST00000710265.1:c.869_870delinsCT	ENSP00000518161.1:p.Val290Ala
ENST00000472832.3:c.869_870delinsCT	ENSP00000483066.2:p.Val290Ala
ENST00000688158.2:n.1604_1605delinsCT
ENST00000688922.2:c.*699_*700delinsCT	ENSP00000508742.2:n.*699_*700delinsCT
ENST00000700021.1:c.824_825delinsCT	ENSP00000514757.1:p.Val275Ala
ENST00000700022.1:c.*208_*209delinsCT	ENSP00000514758.1:n.*208_*209delinsCT
ENST00000700023.1:n.2027_2028delinsCT
ENST00000700024.1:n.2261_2262delinsCT
ENST00000700025.1:n.1638_1639delinsCT
ENST00000700026.1:n.506_507delinsCT
ENST00000700029.1:c.796_797delinsCT
ENST00000706954.1:c.869_870delinsCT	ENSP00000516674.1:p.Val290Ala
ENST00000706955.1:c.*904_*905delinsCT	ENSP00000516675.1:n.*904_*905delinsCT
ENST00000686459.1:c.*455_*456delinsCT	ENSP00000508909.1:n.*455_*456delinsCT
ENST00000688158.1:c.*980_*981delinsCT	ENSP00000509254.1:n.*980_*981delinsCT
ENST00000688308.1:c.869_870delinsCT	ENSP00000508752.1:p.Val290Ala
ENST00000688922.1:c.790_791delinsCT
ENST00000693560.1:c.1388_1389delinsCT	ENSP00000509861.1:p.Val463Ala
ENST00000371953.8:c.869_870delinsCT MANE Select	ENSP00000361021.3:p.Val290Ala
ENST00000371953.7:c.869_870delinsCT	ENSP00000361021.3:p.Val290Ala
ENST00000472832.2:c.296_297delinsCT	ENSP00000483066.1:p.Val99Ala
NM_000314.5:c.869_870delinsCT	NP_000305.3:p.Val290Ala
NM_000314.6:c.869_870delinsCT	NP_000305.3:p.Val290Ala
NM_001304717.2:c.1388_1389delinsCT	NP_001291646.2:p.Val463Ala
NM_001304718.1:c.278_279delinsCT	NP_001291647.1:p.Val93Ala
XM_006717926.2:c.824_825delinsCT	XP_006717989.1:p.Val275Ala
XM_011539981.1:c.869_870delinsCT	XP_011538283.1:p.Val290Ala
XM_011539982.1:c.773_774delinsCT	XP_011538284.1:p.Val258Ala
XR_945791.1:n.1439_1440delinsCT
NM_000314.7:c.869_870delinsCT	NP_000305.3:p.Val290Ala
NM_001304717.5:c.1388_1389delinsCT	NP_001291646.4:p.Val463Ala
NM_001304718.2:c.278_279delinsCT	NP_001291647.1:p.Val93Ala
NM_000314.8:c.869_870delinsCT MANE Select	NP_000305.3:p.Val290Ala