Canonical Allele Identifier: CA891836581

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87933046_87933047delinsAT , CM000672.2:g.87933046_87933047delinsAT	GRCh38
NC_000010.10:g.89692803_89692804delinsAT , CM000672.1:g.89692803_89692804delinsAT	GRCh37
NC_000010.9:g.89682783_89682784delinsAT	NCBI36
NG_007466.2:g.74608_74609delinsAT , LRG_311:g.74608_74609delinsAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.287_288delinsAT	ENSP00000514759.2:p.Pro96His
ENST00000710265.1:c.287_288delinsAT	ENSP00000518161.1:p.Pro96His
ENST00000472832.3:c.287_288delinsAT	ENSP00000483066.2:p.Pro96His
ENST00000688158.2:n.1022_1023delinsAT
ENST00000688922.2:c.*117_*118delinsAT	ENSP00000508742.2:n.*117_*118delinsAT
ENST00000700021.1:c.242_243delinsAT	ENSP00000514757.1:p.Pro81His
ENST00000700022.1:c.287_288delinsAT	ENSP00000514758.1:p.Pro96His
ENST00000700029.1:c.121_122delinsAT
ENST00000706954.1:c.287_288delinsAT	ENSP00000516674.1:p.Pro96His
ENST00000706955.1:c.*322_*323delinsAT	ENSP00000516675.1:n.*322_*323delinsAT
ENST00000686459.1:c.287_288delinsAT	ENSP00000508909.1:p.Pro96His
ENST00000688158.1:c.*398_*399delinsAT	ENSP00000509254.1:n.*398_*399delinsAT
ENST00000688308.1:c.287_288delinsAT	ENSP00000508752.1:p.Pro96His
ENST00000688922.1:c.208_209delinsAT
ENST00000693560.1:c.806_807delinsAT	ENSP00000509861.1:p.Pro269His
ENST00000371953.8:c.287_288delinsAT MANE Select	ENSP00000361021.3:p.Pro96His
ENST00000371953.7:c.287_288delinsAT	ENSP00000361021.3:p.Pro96His
ENST00000498703.1:n.113_114delinsAT
ENST00000610634.1:c.185_186delinsAT	ENSP00000477517.1:p.Pro62His
NM_000314.5:c.287_288delinsAT	NP_000305.3:p.Pro96His
NM_000314.6:c.287_288delinsAT	NP_000305.3:p.Pro96His
NM_001304717.2:c.806_807delinsAT	NP_001291646.2:p.Pro269His
NM_001304718.1:c.-464_-463delinsAT	NP_001291647.1:n.-464_-463delinsAT
XM_006717926.2:c.242_243delinsAT	XP_006717989.1:p.Pro81His
XM_011539981.1:c.287_288delinsAT	XP_011538283.1:p.Pro96His
XM_011539982.1:c.191_192delinsAT	XP_011538284.1:p.Pro64His
XR_945789.1:n.999_1000delinsAT
XR_945790.1:n.999_1000delinsAT
XR_945791.1:n.999_1000delinsAT
NM_000314.7:c.287_288delinsAT	NP_000305.3:p.Pro96His
NM_001304717.5:c.806_807delinsAT	NP_001291646.4:p.Pro269His
NM_001304718.2:c.-464_-463delinsAT	NP_001291647.1:n.-464_-463delinsAT
NM_000314.8:c.287_288delinsAT MANE Select	NP_000305.3:p.Pro96His