Canonical Allele Identifier: CA2579926654

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961090_87961091delinsTT , CM000672.2:g.87961090_87961091delinsTT	GRCh38
NC_000010.10:g.89720847_89720848delinsTT , CM000672.1:g.89720847_89720848delinsTT	GRCh37
NC_000010.9:g.89710827_89710828delinsTT	NCBI36
NG_007466.2:g.102652_102653delinsTT , LRG_311:g.102652_102653delinsTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.1091_1092delinsTT	ENSP00000514759.2:p.Ala364Val
ENST00000710265.1:c.998_999delinsTT	ENSP00000518161.1:p.Ala333Val
ENST00000472832.3:c.998_999delinsTT	ENSP00000483066.2:p.Ala333Val
ENST00000688158.2:n.1733_1734delinsTT
ENST00000688922.2:c.*828_*829delinsTT	ENSP00000508742.2:n.*828_*829delinsTT
ENST00000700021.1:c.953_954delinsTT	ENSP00000514757.1:p.Ala318Val
ENST00000700022.1:c.*337_*338delinsTT	ENSP00000514758.1:n.*337_*338delinsTT
ENST00000700023.1:n.2156_2157delinsTT
ENST00000700024.1:n.2390_2391delinsTT
ENST00000700025.1:n.1767_1768delinsTT
ENST00000700026.1:n.635_636delinsTT
ENST00000706954.1:c.998_999delinsTT	ENSP00000516674.1:p.Ala333Val
ENST00000706955.1:c.*1033_*1034delinsTT	ENSP00000516675.1:n.*1033_*1034delinsTT
ENST00000686459.1:c.*584_*585delinsTT	ENSP00000508909.1:n.*584_*585delinsTT
ENST00000688158.1:c.*1109_*1110delinsTT	ENSP00000509254.1:n.*1109_*1110delinsTT
ENST00000688308.1:c.998_999delinsTT	ENSP00000508752.1:p.Ala333Val
ENST00000688922.1:c.919_920delinsTT
ENST00000693560.1:c.1517_1518delinsTT	ENSP00000509861.1:p.Ala506Val
ENST00000371953.8:c.998_999delinsTT MANE Select	ENSP00000361021.3:p.Ala333Val
ENST00000371953.7:c.998_999delinsTT	ENSP00000361021.3:p.Ala333Val
ENST00000472832.2:c.425_426delinsTT	ENSP00000483066.1:p.Ala142Val
NM_000314.5:c.998_999delinsTT	NP_000305.3:p.Ala333Val
NM_000314.6:c.998_999delinsTT	NP_000305.3:p.Ala333Val
NM_001304717.2:c.1517_1518delinsTT	NP_001291646.2:p.Ala506Val
NM_001304718.1:c.407_408delinsTT	NP_001291647.1:p.Ala136Val
XM_006717926.2:c.953_954delinsTT	XP_006717989.1:p.Ala318Val
XM_011539981.1:c.998_999delinsTT	XP_011538283.1:p.Ala333Val
XM_011539982.1:c.902_903delinsTT	XP_011538284.1:p.Ala301Val
XR_945791.1:n.1568_1569delinsTT
NM_000314.7:c.998_999delinsTT	NP_000305.3:p.Ala333Val
NM_001304717.5:c.1517_1518delinsTT	NP_001291646.4:p.Ala506Val
NM_001304718.2:c.407_408delinsTT	NP_001291647.1:p.Ala136Val
NM_000314.8:c.998_999delinsTT MANE Select	NP_000305.3:p.Ala333Val