Canonical Allele Identifier: CA891839418

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957877_87957878delinsAT , CM000672.2:g.87957877_87957878delinsAT	GRCh38
NC_000010.10:g.89717634_89717635delinsAT , CM000672.1:g.89717634_89717635delinsAT	GRCh37
NC_000010.9:g.89707614_89707615delinsAT	NCBI36
NG_007466.2:g.99439_99440delinsAT , LRG_311:g.99439_99440delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.659_660delinsAT	ENSP00000514759.2:p.Leu220His
ENST00000710265.1:c.659_660delinsAT	ENSP00000518161.1:p.Leu220His
ENST00000472832.3:c.659_660delinsAT	ENSP00000483066.2:p.Leu220His
ENST00000688158.2:n.1394_1395delinsAT
ENST00000688922.2:c.*489_*490delinsAT	ENSP00000508742.2:n.*489_*490delinsAT
ENST00000700021.1:c.614_615delinsAT	ENSP00000514757.1:p.Leu205His
ENST00000700022.1:c.517_518delinsAT	ENSP00000514758.1:p.Ter173Ile
ENST00000700023.1:n.1817_1818delinsAT
ENST00000700024.1:n.2051_2052delinsAT
ENST00000700025.1:n.1428_1429delinsAT
ENST00000700026.1:n.296_297delinsAT
ENST00000700029.1:c.493_494delinsAT
ENST00000706954.1:c.659_660delinsAT	ENSP00000516674.1:p.Leu220His
ENST00000706955.1:c.*694_*695delinsAT	ENSP00000516675.1:n.*694_*695delinsAT
ENST00000686459.1:c.*245_*246delinsAT	ENSP00000508909.1:n.*245_*246delinsAT
ENST00000688158.1:c.*770_*771delinsAT	ENSP00000509254.1:n.*770_*771delinsAT
ENST00000688308.1:c.659_660delinsAT	ENSP00000508752.1:p.Leu220His
ENST00000688922.1:c.580_581delinsAT
ENST00000693560.1:c.1178_1179delinsAT	ENSP00000509861.1:p.Leu393His
ENST00000371953.8:c.659_660delinsAT MANE Select	ENSP00000361021.3:p.Leu220His
ENST00000371953.7:c.659_660delinsAT	ENSP00000361021.3:p.Leu220His
ENST00000472832.2:c.86_87delinsAT	ENSP00000483066.1:p.Leu29His
NM_000314.5:c.659_660delinsAT	NP_000305.3:p.Leu220His
NM_000314.6:c.659_660delinsAT	NP_000305.3:p.Leu220His
NM_001304717.2:c.1178_1179delinsAT	NP_001291646.2:p.Leu393His
NM_001304718.1:c.68_69delinsAT	NP_001291647.1:p.Leu23His
XM_006717926.2:c.614_615delinsAT	XP_006717989.1:p.Leu205His
XM_011539981.1:c.659_660delinsAT	XP_011538283.1:p.Leu220His
XM_011539982.1:c.563_564delinsAT	XP_011538284.1:p.Leu188His
XR_945791.1:n.1229_1230delinsAT
NM_000314.7:c.659_660delinsAT	NP_000305.3:p.Leu220His
NM_001304717.5:c.1178_1179delinsAT	NP_001291646.4:p.Leu393His
NM_001304718.2:c.68_69delinsAT	NP_001291647.1:p.Leu23His
NM_000314.8:c.659_660delinsAT MANE Select	NP_000305.3:p.Leu220His