Canonical Allele Identifier: CA2579926645

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961090_87961091delinsAT , CM000672.2:g.87961090_87961091delinsAT	GRCh38
NC_000010.10:g.89720847_89720848delinsAT , CM000672.1:g.89720847_89720848delinsAT	GRCh37
NC_000010.9:g.89710827_89710828delinsAT	NCBI36
NG_007466.2:g.102652_102653delinsAT , LRG_311:g.102652_102653delinsAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.1091_1092delinsAT	ENSP00000514759.2:p.Ala364Asp
ENST00000710265.1:c.998_999delinsAT	ENSP00000518161.1:p.Ala333Asp
ENST00000472832.3:c.998_999delinsAT	ENSP00000483066.2:p.Ala333Asp
ENST00000688158.2:n.1733_1734delinsAT
ENST00000688922.2:c.*828_*829delinsAT	ENSP00000508742.2:n.*828_*829delinsAT
ENST00000700021.1:c.953_954delinsAT	ENSP00000514757.1:p.Ala318Asp
ENST00000700022.1:c.*337_*338delinsAT	ENSP00000514758.1:n.*337_*338delinsAT
ENST00000700023.1:n.2156_2157delinsAT
ENST00000700024.1:n.2390_2391delinsAT
ENST00000700025.1:n.1767_1768delinsAT
ENST00000700026.1:n.635_636delinsAT
ENST00000706954.1:c.998_999delinsAT	ENSP00000516674.1:p.Ala333Asp
ENST00000706955.1:c.*1033_*1034delinsAT	ENSP00000516675.1:n.*1033_*1034delinsAT
ENST00000686459.1:c.*584_*585delinsAT	ENSP00000508909.1:n.*584_*585delinsAT
ENST00000688158.1:c.*1109_*1110delinsAT	ENSP00000509254.1:n.*1109_*1110delinsAT
ENST00000688308.1:c.998_999delinsAT	ENSP00000508752.1:p.Ala333Asp
ENST00000688922.1:c.919_920delinsAT
ENST00000693560.1:c.1517_1518delinsAT	ENSP00000509861.1:p.Ala506Asp
ENST00000371953.8:c.998_999delinsAT MANE Select	ENSP00000361021.3:p.Ala333Asp
ENST00000371953.7:c.998_999delinsAT	ENSP00000361021.3:p.Ala333Asp
ENST00000472832.2:c.425_426delinsAT	ENSP00000483066.1:p.Ala142Asp
NM_000314.5:c.998_999delinsAT	NP_000305.3:p.Ala333Asp
NM_000314.6:c.998_999delinsAT	NP_000305.3:p.Ala333Asp
NM_001304717.2:c.1517_1518delinsAT	NP_001291646.2:p.Ala506Asp
NM_001304718.1:c.407_408delinsAT	NP_001291647.1:p.Ala136Asp
XM_006717926.2:c.953_954delinsAT	XP_006717989.1:p.Ala318Asp
XM_011539981.1:c.998_999delinsAT	XP_011538283.1:p.Ala333Asp
XM_011539982.1:c.902_903delinsAT	XP_011538284.1:p.Ala301Asp
XR_945791.1:n.1568_1569delinsAT
NM_000314.7:c.998_999delinsAT	NP_000305.3:p.Ala333Asp
NM_001304717.5:c.1517_1518delinsAT	NP_001291646.4:p.Ala506Asp
NM_001304718.2:c.407_408delinsAT	NP_001291647.1:p.Ala136Asp
NM_000314.8:c.998_999delinsAT MANE Select	NP_000305.3:p.Ala333Asp