Canonical Allele Identifier: CA891835228

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960961_87960962delinsAT , CM000672.2:g.87960961_87960962delinsAT	GRCh38
NC_000010.10:g.89720718_89720719delinsAT , CM000672.1:g.89720718_89720719delinsAT	GRCh37
NC_000010.9:g.89710698_89710699delinsAT	NCBI36
NG_007466.2:g.102523_102524delinsAT , LRG_311:g.102523_102524delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.962_963delinsAT	ENSP00000514759.2:p.Val321Asp
ENST00000710265.1:c.869_870delinsAT	ENSP00000518161.1:p.Val290Asp
ENST00000472832.3:c.869_870delinsAT	ENSP00000483066.2:p.Val290Asp
ENST00000688158.2:n.1604_1605delinsAT
ENST00000688922.2:c.*699_*700delinsAT	ENSP00000508742.2:n.*699_*700delinsAT
ENST00000700021.1:c.824_825delinsAT	ENSP00000514757.1:p.Val275Asp
ENST00000700022.1:c.*208_*209delinsAT	ENSP00000514758.1:n.*208_*209delinsAT
ENST00000700023.1:n.2027_2028delinsAT
ENST00000700024.1:n.2261_2262delinsAT
ENST00000700025.1:n.1638_1639delinsAT
ENST00000700026.1:n.506_507delinsAT
ENST00000700029.1:c.796_797delinsAT
ENST00000706954.1:c.869_870delinsAT	ENSP00000516674.1:p.Val290Asp
ENST00000706955.1:c.*904_*905delinsAT	ENSP00000516675.1:n.*904_*905delinsAT
ENST00000686459.1:c.*455_*456delinsAT	ENSP00000508909.1:n.*455_*456delinsAT
ENST00000688158.1:c.*980_*981delinsAT	ENSP00000509254.1:n.*980_*981delinsAT
ENST00000688308.1:c.869_870delinsAT	ENSP00000508752.1:p.Val290Asp
ENST00000688922.1:c.790_791delinsAT
ENST00000693560.1:c.1388_1389delinsAT	ENSP00000509861.1:p.Val463Asp
ENST00000371953.8:c.869_870delinsAT MANE Select	ENSP00000361021.3:p.Val290Asp
ENST00000371953.7:c.869_870delinsAT	ENSP00000361021.3:p.Val290Asp
ENST00000472832.2:c.296_297delinsAT	ENSP00000483066.1:p.Val99Asp
NM_000314.5:c.869_870delinsAT	NP_000305.3:p.Val290Asp
NM_000314.6:c.869_870delinsAT	NP_000305.3:p.Val290Asp
NM_001304717.2:c.1388_1389delinsAT	NP_001291646.2:p.Val463Asp
NM_001304718.1:c.278_279delinsAT	NP_001291647.1:p.Val93Asp
XM_006717926.2:c.824_825delinsAT	XP_006717989.1:p.Val275Asp
XM_011539981.1:c.869_870delinsAT	XP_011538283.1:p.Val290Asp
XM_011539982.1:c.773_774delinsAT	XP_011538284.1:p.Val258Asp
XR_945791.1:n.1439_1440delinsAT
NM_000314.7:c.869_870delinsAT	NP_000305.3:p.Val290Asp
NM_001304717.5:c.1388_1389delinsAT	NP_001291646.4:p.Val463Asp
NM_001304718.2:c.278_279delinsAT	NP_001291647.1:p.Val93Asp
NM_000314.8:c.869_870delinsAT MANE Select	NP_000305.3:p.Val290Asp