Canonical Allele Identifier: CA891841376

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961090_87961091delinsAA , CM000672.2:g.87961090_87961091delinsAA	GRCh38
NC_000010.10:g.89720847_89720848delinsAA , CM000672.1:g.89720847_89720848delinsAA	GRCh37
NC_000010.9:g.89710827_89710828delinsAA	NCBI36
NG_007466.2:g.102652_102653delinsAA , LRG_311:g.102652_102653delinsAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.1091_1092delinsAA	ENSP00000514759.2:p.Ala364Glu
ENST00000710265.1:c.998_999delinsAA	ENSP00000518161.1:p.Ala333Glu
ENST00000472832.3:c.998_999delinsAA	ENSP00000483066.2:p.Ala333Glu
ENST00000688158.2:n.1733_1734delinsAA
ENST00000688922.2:c.*828_*829delinsAA	ENSP00000508742.2:n.*828_*829delinsAA
ENST00000700021.1:c.953_954delinsAA	ENSP00000514757.1:p.Ala318Glu
ENST00000700022.1:c.*337_*338delinsAA	ENSP00000514758.1:n.*337_*338delinsAA
ENST00000700023.1:n.2156_2157delinsAA
ENST00000700024.1:n.2390_2391delinsAA
ENST00000700025.1:n.1767_1768delinsAA
ENST00000700026.1:n.635_636delinsAA
ENST00000706954.1:c.998_999delinsAA	ENSP00000516674.1:p.Ala333Glu
ENST00000706955.1:c.*1033_*1034delinsAA	ENSP00000516675.1:n.*1033_*1034delinsAA
ENST00000686459.1:c.*584_*585delinsAA	ENSP00000508909.1:n.*584_*585delinsAA
ENST00000688158.1:c.*1109_*1110delinsAA	ENSP00000509254.1:n.*1109_*1110delinsAA
ENST00000688308.1:c.998_999delinsAA	ENSP00000508752.1:p.Ala333Glu
ENST00000688922.1:c.919_920delinsAA
ENST00000693560.1:c.1517_1518delinsAA	ENSP00000509861.1:p.Ala506Glu
ENST00000371953.8:c.998_999delinsAA MANE Select	ENSP00000361021.3:p.Ala333Glu
ENST00000371953.7:c.998_999delinsAA	ENSP00000361021.3:p.Ala333Glu
ENST00000472832.2:c.425_426delinsAA	ENSP00000483066.1:p.Ala142Glu
NM_000314.5:c.998_999delinsAA	NP_000305.3:p.Ala333Glu
NM_000314.6:c.998_999delinsAA	NP_000305.3:p.Ala333Glu
NM_001304717.2:c.1517_1518delinsAA	NP_001291646.2:p.Ala506Glu
NM_001304718.1:c.407_408delinsAA	NP_001291647.1:p.Ala136Glu
XM_006717926.2:c.953_954delinsAA	XP_006717989.1:p.Ala318Glu
XM_011539981.1:c.998_999delinsAA	XP_011538283.1:p.Ala333Glu
XM_011539982.1:c.902_903delinsAA	XP_011538284.1:p.Ala301Glu
XR_945791.1:n.1568_1569delinsAA
NM_000314.7:c.998_999delinsAA	NP_000305.3:p.Ala333Glu
NM_001304717.5:c.1517_1518delinsAA	NP_001291646.4:p.Ala506Glu
NM_001304718.2:c.407_408delinsAA	NP_001291647.1:p.Ala136Glu
NM_000314.8:c.998_999delinsAA MANE Select	NP_000305.3:p.Ala333Glu