Canonical Allele Identifier: CA891835230

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960961_87960962delinsGT , CM000672.2:g.87960961_87960962delinsGT	GRCh38
NC_000010.10:g.89720718_89720719delinsGT , CM000672.1:g.89720718_89720719delinsGT	GRCh37
NC_000010.9:g.89710698_89710699delinsGT	NCBI36
NG_007466.2:g.102523_102524delinsGT , LRG_311:g.102523_102524delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.962_963delinsGT	ENSP00000514759.2:p.Val321Gly
ENST00000710265.1:c.869_870delinsGT	ENSP00000518161.1:p.Val290Gly
ENST00000472832.3:c.869_870delinsGT	ENSP00000483066.2:p.Val290Gly
ENST00000688158.2:n.1604_1605delinsGT
ENST00000688922.2:c.*699_*700delinsGT	ENSP00000508742.2:n.*699_*700delinsGT
ENST00000700021.1:c.824_825delinsGT	ENSP00000514757.1:p.Val275Gly
ENST00000700022.1:c.*208_*209delinsGT	ENSP00000514758.1:n.*208_*209delinsGT
ENST00000700023.1:n.2027_2028delinsGT
ENST00000700024.1:n.2261_2262delinsGT
ENST00000700025.1:n.1638_1639delinsGT
ENST00000700026.1:n.506_507delinsGT
ENST00000700029.1:c.796_797delinsGT
ENST00000706954.1:c.869_870delinsGT	ENSP00000516674.1:p.Val290Gly
ENST00000706955.1:c.*904_*905delinsGT	ENSP00000516675.1:n.*904_*905delinsGT
ENST00000686459.1:c.*455_*456delinsGT	ENSP00000508909.1:n.*455_*456delinsGT
ENST00000688158.1:c.*980_*981delinsGT	ENSP00000509254.1:n.*980_*981delinsGT
ENST00000688308.1:c.869_870delinsGT	ENSP00000508752.1:p.Val290Gly
ENST00000688922.1:c.790_791delinsGT
ENST00000693560.1:c.1388_1389delinsGT	ENSP00000509861.1:p.Val463Gly
ENST00000371953.8:c.869_870delinsGT MANE Select	ENSP00000361021.3:p.Val290Gly
ENST00000371953.7:c.869_870delinsGT	ENSP00000361021.3:p.Val290Gly
ENST00000472832.2:c.296_297delinsGT	ENSP00000483066.1:p.Val99Gly
NM_000314.5:c.869_870delinsGT	NP_000305.3:p.Val290Gly
NM_000314.6:c.869_870delinsGT	NP_000305.3:p.Val290Gly
NM_001304717.2:c.1388_1389delinsGT	NP_001291646.2:p.Val463Gly
NM_001304718.1:c.278_279delinsGT	NP_001291647.1:p.Val93Gly
XM_006717926.2:c.824_825delinsGT	XP_006717989.1:p.Val275Gly
XM_011539981.1:c.869_870delinsGT	XP_011538283.1:p.Val290Gly
XM_011539982.1:c.773_774delinsGT	XP_011538284.1:p.Val258Gly
XR_945791.1:n.1439_1440delinsGT
NM_000314.7:c.869_870delinsGT	NP_000305.3:p.Val290Gly
NM_001304717.5:c.1388_1389delinsGT	NP_001291646.4:p.Val463Gly
NM_001304718.2:c.278_279delinsGT	NP_001291647.1:p.Val93Gly
NM_000314.8:c.869_870delinsGT MANE Select	NP_000305.3:p.Val290Gly