Canonical Allele Identifier: CA891839312

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957855_87957856delinsTT , CM000672.2:g.87957855_87957856delinsTT	GRCh38
NC_000010.10:g.89717612_89717613delinsTT , CM000672.1:g.89717612_89717613delinsTT	GRCh37
NC_000010.9:g.89707592_89707593delinsTT	NCBI36
NG_007466.2:g.99417_99418delinsTT , LRG_311:g.99417_99418delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.637_638delinsTT	ENSP00000514759.2:p.Pro213Phe
ENST00000710265.1:c.637_638delinsTT	ENSP00000518161.1:p.Pro213Phe
ENST00000472832.3:c.637_638delinsTT	ENSP00000483066.2:p.Pro213Phe
ENST00000688158.2:n.1372_1373delinsTT
ENST00000688922.2:c.*467_*468delinsTT	ENSP00000508742.2:n.*467_*468delinsTT
ENST00000700021.1:c.592_593delinsTT	ENSP00000514757.1:p.Pro198Phe
ENST00000700022.1:c.495_496delinsTT	ENSP00000514758.1:p.Leu166Phe
ENST00000700023.1:n.1795_1796delinsTT
ENST00000700024.1:n.2029_2030delinsTT
ENST00000700025.1:n.1406_1407delinsTT
ENST00000700026.1:n.274_275delinsTT
ENST00000700029.1:c.471_472delinsTT
ENST00000706954.1:c.637_638delinsTT	ENSP00000516674.1:p.Pro213Phe
ENST00000706955.1:c.*672_*673delinsTT	ENSP00000516675.1:n.*672_*673delinsTT
ENST00000686459.1:c.*223_*224delinsTT	ENSP00000508909.1:n.*223_*224delinsTT
ENST00000688158.1:c.*748_*749delinsTT	ENSP00000509254.1:n.*748_*749delinsTT
ENST00000688308.1:c.637_638delinsTT	ENSP00000508752.1:p.Pro213Phe
ENST00000688922.1:c.558_559delinsTT
ENST00000693560.1:c.1156_1157delinsTT	ENSP00000509861.1:p.Pro386Phe
ENST00000371953.8:c.637_638delinsTT MANE Select	ENSP00000361021.3:p.Pro213Phe
ENST00000371953.7:c.637_638delinsTT	ENSP00000361021.3:p.Pro213Phe
ENST00000472832.2:c.64_65delinsTT	ENSP00000483066.1:p.Pro22Phe
NM_000314.5:c.637_638delinsTT	NP_000305.3:p.Pro213Phe
NM_000314.6:c.637_638delinsTT	NP_000305.3:p.Pro213Phe
NM_001304717.2:c.1156_1157delinsTT	NP_001291646.2:p.Pro386Phe
NM_001304718.1:c.46_47delinsTT	NP_001291647.1:p.Pro16Phe
XM_006717926.2:c.592_593delinsTT	XP_006717989.1:p.Pro198Phe
XM_011539981.1:c.637_638delinsTT	XP_011538283.1:p.Pro213Phe
XM_011539982.1:c.541_542delinsTT	XP_011538284.1:p.Pro181Phe
XR_945791.1:n.1207_1208delinsTT
NM_000314.7:c.637_638delinsTT	NP_000305.3:p.Pro213Phe
NM_001304717.5:c.1156_1157delinsTT	NP_001291646.4:p.Pro386Phe
NM_001304718.2:c.46_47delinsTT	NP_001291647.1:p.Pro16Phe
NM_000314.8:c.637_638delinsTT MANE Select	NP_000305.3:p.Pro213Phe