Canonical Allele Identifier: CA2542647396

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965516_87965523del , CM000672.2:g.87965516_87965523del	GRCh38
NC_000010.10:g.89725273_89725280del , CM000672.1:g.89725273_89725280del	GRCh37
NC_000010.9:g.89715253_89715260del	NCBI36
NG_007466.2:g.107078_107085del , LRG_311:g.107078_107085del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.*44_*51del	ENSP00000514759.2:n.*44_*51del
ENST00000710265.1:c.*285_*292del	ENSP00000518161.1:n.*285_*292del
ENST00000688158.2:n.1991_1998del
ENST00000688922.2:c.*1086_*1093del	ENSP00000508742.2:n.*1086_*1093del
ENST00000700021.1:c.*44_*51del	ENSP00000514757.1:n.*44_*51del
ENST00000700022.1:c.*595_*602del	ENSP00000514758.1:n.*595_*602del
ENST00000700023.1:n.2414_2421del
ENST00000700024.1:n.2648_2655del
ENST00000706954.1:c.*44_*51del	ENSP00000516674.1:n.*44_*51del
ENST00000706955.1:c.*1291_*1298del	ENSP00000516675.1:n.*1291_*1298del
ENST00000686459.1:c.*842_*849del	ENSP00000508909.1:n.*842_*849del
ENST00000688158.1:c.*1367_*1374del	ENSP00000509254.1:n.*1367_*1374del
ENST00000688308.1:c.*44_*51del	ENSP00000508752.1:n.*44_*51del
ENST00000688922.1:c.1177_1184del
ENST00000693560.1:c.*44_*51del	ENSP00000509861.1:n.*44_*51del
ENST00000371953.8:c.*44_*51del MANE Select	ENSP00000361021.3:n.*44_*51del
ENST00000371953.7:c.*44_*51del	ENSP00000361021.3:n.*44_*51del
NM_000314.5:c.*44_*51del	NP_000305.3:n.*44_*51del
NM_000314.6:c.*44_*51del	NP_000305.3:n.*44_*51del
NM_001304717.2:c.*44_*51del	NP_001291646.2:n.*44_*51del
NM_001304718.1:c.*44_*51del	NP_001291647.1:n.*44_*51del
XM_006717926.2:c.*44_*51del	XP_006717989.1:n.*44_*51del
XM_011539982.1:c.*44_*51del	XP_011538284.1:n.*44_*51del
XR_945791.1:n.1826_1833del
NM_000314.7:c.*44_*51del	NP_000305.3:n.*44_*51del
NM_001304717.5:c.*44_*51del	NP_001291646.4:n.*44_*51del
NM_001304718.2:c.*44_*51del	NP_001291647.1:n.*44_*51del
NM_000314.8:c.*44_*51del MANE Select	NP_000305.3:n.*44_*51del