Canonical Allele Identifier: CA891840311

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957855_87957857delinsCCT , CM000672.2:g.87957855_87957857delinsCCT	GRCh38
NC_000010.10:g.89717612_89717614delinsCCT , CM000672.1:g.89717612_89717614delinsCCT	GRCh37
NC_000010.9:g.89707592_89707594delinsCCT	NCBI36
NG_007466.2:g.99417_99419delinsCCT , LRG_311:g.99417_99419delinsCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.637_639delinsCCT	ENSP00000514759.2:p.Pro213=
ENST00000710265.1:c.637_639delinsCCT	ENSP00000518161.1:p.Pro213=
ENST00000472832.3:c.637_639delinsCCT	ENSP00000483066.2:p.Pro213=
ENST00000688158.2:n.1372_1374delinsCCT
ENST00000688922.2:c.*467_*469delinsCCT	ENSP00000508742.2:n.*467_*469delinsCCT
ENST00000700021.1:c.592_594delinsCCT	ENSP00000514757.1:p.Pro198=
ENST00000700022.1:c.495_497delinsCCT	ENSP00000514758.1:p.Ile165=
ENST00000700023.1:n.1795_1797delinsCCT
ENST00000700024.1:n.2029_2031delinsCCT
ENST00000700025.1:n.1406_1408delinsCCT
ENST00000700026.1:n.274_276delinsCCT
ENST00000700029.1:c.471_473delinsCCT
ENST00000706954.1:c.637_639delinsCCT	ENSP00000516674.1:p.Pro213=
ENST00000706955.1:c.*672_*674delinsCCT	ENSP00000516675.1:n.*672_*674delinsCCT
ENST00000686459.1:c.*223_*225delinsCCT	ENSP00000508909.1:n.*223_*225delinsCCT
ENST00000688158.1:c.*748_*750delinsCCT	ENSP00000509254.1:n.*748_*750delinsCCT
ENST00000688308.1:c.637_639delinsCCT	ENSP00000508752.1:p.Pro213=
ENST00000688922.1:c.558_560delinsCCT
ENST00000693560.1:c.1156_1158delinsCCT	ENSP00000509861.1:p.Pro386=
ENST00000371953.8:c.637_639delinsCCT MANE Select	ENSP00000361021.3:p.Pro213=
ENST00000371953.7:c.637_639delinsCCT	ENSP00000361021.3:p.Pro213=
ENST00000472832.2:c.64_66delinsCCT	ENSP00000483066.1:p.Pro22=
NM_000314.5:c.637_639delinsCCT	NP_000305.3:p.Pro213=
NM_000314.6:c.637_639delinsCCT	NP_000305.3:p.Pro213=
NM_001304717.2:c.1156_1158delinsCCT	NP_001291646.2:p.Pro386=
NM_001304718.1:c.46_48delinsCCT	NP_001291647.1:p.Pro16=
XM_006717926.2:c.592_594delinsCCT	XP_006717989.1:p.Pro198=
XM_011539981.1:c.637_639delinsCCT	XP_011538283.1:p.Pro213=
XM_011539982.1:c.541_543delinsCCT	XP_011538284.1:p.Pro181=
XR_945791.1:n.1207_1209delinsCCT
NM_000314.7:c.637_639delinsCCT	NP_000305.3:p.Pro213=
NM_001304717.5:c.1156_1158delinsCCT	NP_001291646.4:p.Pro386=
NM_001304718.2:c.46_48delinsCCT	NP_001291647.1:p.Pro16=
NM_000314.8:c.637_639delinsCCT MANE Select	NP_000305.3:p.Pro213=