Canonical Allele Identifier: CA891835215

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960960_87960962delinsTAT , CM000672.2:g.87960960_87960962delinsTAT	GRCh38
NC_000010.10:g.89720717_89720719delinsTAT , CM000672.1:g.89720717_89720719delinsTAT	GRCh37
NC_000010.9:g.89710697_89710699delinsTAT	NCBI36
NG_007466.2:g.102522_102524delinsTAT , LRG_311:g.102522_102524delinsTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.961_963delinsTAT	ENSP00000514759.2:p.Val321Tyr
ENST00000710265.1:c.868_870delinsTAT	ENSP00000518161.1:p.Val290Tyr
ENST00000472832.3:c.868_870delinsTAT	ENSP00000483066.2:p.Val290Tyr
ENST00000688158.2:n.1603_1605delinsTAT
ENST00000688922.2:c.*698_*700delinsTAT	ENSP00000508742.2:n.*698_*700delinsTAT
ENST00000700021.1:c.823_825delinsTAT	ENSP00000514757.1:p.Val275Tyr
ENST00000700022.1:c.*207_*209delinsTAT	ENSP00000514758.1:n.*207_*209delinsTAT
ENST00000700023.1:n.2026_2028delinsTAT
ENST00000700024.1:n.2260_2262delinsTAT
ENST00000700025.1:n.1637_1639delinsTAT
ENST00000700026.1:n.505_507delinsTAT
ENST00000700029.1:c.795_797delinsTAT
ENST00000706954.1:c.868_870delinsTAT	ENSP00000516674.1:p.Val290Tyr
ENST00000706955.1:c.*903_*905delinsTAT	ENSP00000516675.1:n.*903_*905delinsTAT
ENST00000686459.1:c.*454_*456delinsTAT	ENSP00000508909.1:n.*454_*456delinsTAT
ENST00000688158.1:c.*979_*981delinsTAT	ENSP00000509254.1:n.*979_*981delinsTAT
ENST00000688308.1:c.868_870delinsTAT	ENSP00000508752.1:p.Val290Tyr
ENST00000688922.1:c.789_791delinsTAT
ENST00000693560.1:c.1387_1389delinsTAT	ENSP00000509861.1:p.Val463Tyr
ENST00000371953.8:c.868_870delinsTAT MANE Select	ENSP00000361021.3:p.Val290Tyr
ENST00000371953.7:c.868_870delinsTAT	ENSP00000361021.3:p.Val290Tyr
ENST00000472832.2:c.295_297delinsTAT	ENSP00000483066.1:p.Val99Tyr
NM_000314.5:c.868_870delinsTAT	NP_000305.3:p.Val290Tyr
NM_000314.6:c.868_870delinsTAT	NP_000305.3:p.Val290Tyr
NM_001304717.2:c.1387_1389delinsTAT	NP_001291646.2:p.Val463Tyr
NM_001304718.1:c.277_279delinsTAT	NP_001291647.1:p.Val93Tyr
XM_006717926.2:c.823_825delinsTAT	XP_006717989.1:p.Val275Tyr
XM_011539981.1:c.868_870delinsTAT	XP_011538283.1:p.Val290Tyr
XM_011539982.1:c.772_774delinsTAT	XP_011538284.1:p.Val258Tyr
XR_945791.1:n.1438_1440delinsTAT
NM_000314.7:c.868_870delinsTAT	NP_000305.3:p.Val290Tyr
NM_001304717.5:c.1387_1389delinsTAT	NP_001291646.4:p.Val463Tyr
NM_001304718.2:c.277_279delinsTAT	NP_001291647.1:p.Val93Tyr
NM_000314.8:c.868_870delinsTAT MANE Select	NP_000305.3:p.Val290Tyr