Canonical Allele Identifier: CA891835210

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960960_87960962delinsAAT , CM000672.2:g.87960960_87960962delinsAAT	GRCh38
NC_000010.10:g.89720717_89720719delinsAAT , CM000672.1:g.89720717_89720719delinsAAT	GRCh37
NC_000010.9:g.89710697_89710699delinsAAT	NCBI36
NG_007466.2:g.102522_102524delinsAAT , LRG_311:g.102522_102524delinsAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.961_963delinsAAT	ENSP00000514759.2:p.Val321Asn
ENST00000710265.1:c.868_870delinsAAT	ENSP00000518161.1:p.Val290Asn
ENST00000472832.3:c.868_870delinsAAT	ENSP00000483066.2:p.Val290Asn
ENST00000688158.2:n.1603_1605delinsAAT
ENST00000688922.2:c.*698_*700delinsAAT	ENSP00000508742.2:n.*698_*700delinsAAT
ENST00000700021.1:c.823_825delinsAAT	ENSP00000514757.1:p.Val275Asn
ENST00000700022.1:c.*207_*209delinsAAT	ENSP00000514758.1:n.*207_*209delinsAAT
ENST00000700023.1:n.2026_2028delinsAAT
ENST00000700024.1:n.2260_2262delinsAAT
ENST00000700025.1:n.1637_1639delinsAAT
ENST00000700026.1:n.505_507delinsAAT
ENST00000700029.1:c.795_797delinsAAT
ENST00000706954.1:c.868_870delinsAAT	ENSP00000516674.1:p.Val290Asn
ENST00000706955.1:c.*903_*905delinsAAT	ENSP00000516675.1:n.*903_*905delinsAAT
ENST00000686459.1:c.*454_*456delinsAAT	ENSP00000508909.1:n.*454_*456delinsAAT
ENST00000688158.1:c.*979_*981delinsAAT	ENSP00000509254.1:n.*979_*981delinsAAT
ENST00000688308.1:c.868_870delinsAAT	ENSP00000508752.1:p.Val290Asn
ENST00000688922.1:c.789_791delinsAAT
ENST00000693560.1:c.1387_1389delinsAAT	ENSP00000509861.1:p.Val463Asn
ENST00000371953.8:c.868_870delinsAAT MANE Select	ENSP00000361021.3:p.Val290Asn
ENST00000371953.7:c.868_870delinsAAT	ENSP00000361021.3:p.Val290Asn
ENST00000472832.2:c.295_297delinsAAT	ENSP00000483066.1:p.Val99Asn
NM_000314.5:c.868_870delinsAAT	NP_000305.3:p.Val290Asn
NM_000314.6:c.868_870delinsAAT	NP_000305.3:p.Val290Asn
NM_001304717.2:c.1387_1389delinsAAT	NP_001291646.2:p.Val463Asn
NM_001304718.1:c.277_279delinsAAT	NP_001291647.1:p.Val93Asn
XM_006717926.2:c.823_825delinsAAT	XP_006717989.1:p.Val275Asn
XM_011539981.1:c.868_870delinsAAT	XP_011538283.1:p.Val290Asn
XM_011539982.1:c.772_774delinsAAT	XP_011538284.1:p.Val258Asn
XR_945791.1:n.1438_1440delinsAAT
NM_000314.7:c.868_870delinsAAT	NP_000305.3:p.Val290Asn
NM_001304717.5:c.1387_1389delinsAAT	NP_001291646.4:p.Val463Asn
NM_001304718.2:c.277_279delinsAAT	NP_001291647.1:p.Val93Asn
NM_000314.8:c.868_870delinsAAT MANE Select	NP_000305.3:p.Val290Asn