Canonical Allele Identifier: CA891840691

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87864545_87864546delinsGG , CM000672.2:g.87864545_87864546delinsGG	GRCh38
NC_000010.10:g.89624302_89624303delinsGG , CM000672.1:g.89624302_89624303delinsGG	GRCh37
NC_000010.9:g.89614282_89614283delinsGG	NCBI36
NG_007466.2:g.6107_6108delinsGG , LRG_311:g.6107_6108delinsGG
NG_033079.1:g.3892_3893delinsCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.76_77delinsGG	ENSP00000514759.2:p.Thr26Gly
ENST00000710265.1:c.76_77delinsGG	ENSP00000518161.1:p.Thr26Gly
ENST00000472832.3:c.76_77delinsGG	ENSP00000483066.2:p.Thr26Gly
ENST00000688922.2:c.76_77delinsGG	ENSP00000508742.2:p.Thr26Gly
ENST00000700021.1:c.76_77delinsGG	ENSP00000514757.1:p.Thr26Gly
ENST00000700022.1:c.76_77delinsGG	ENSP00000514758.1:p.Thr26Gly
ENST00000706954.1:c.76_77delinsGG	ENSP00000516674.1:p.Thr26Gly
ENST00000706955.1:c.76_77delinsGG	ENSP00000516675.1:p.Thr26Gly
ENST00000686459.1:c.76_77delinsGG	ENSP00000508909.1:p.Thr26Gly
ENST00000688158.1:c.76_77delinsGG	ENSP00000509254.1:p.Thr26Gly
ENST00000688308.1:c.76_77delinsGG	ENSP00000508752.1:p.Thr26Gly
ENST00000693560.1:c.595_596delinsGG	ENSP00000509861.1:p.Thr199Gly
ENST00000371953.8:c.76_77delinsGG MANE Select	ENSP00000361021.3:p.Thr26Gly
ENST00000371953.7:c.76_77delinsGG	ENSP00000361021.3:p.Thr26Gly
ENST00000462694.1:n.78_79delinsGG
ENST00000487939.1:n.97_98delinsGG
ENST00000610634.1:c.-27_-26delinsGG	ENSP00000477517.1:n.-27_-26delinsGG
ENST00000618586.1:n.45_46delinsGG
NM_000314.5:c.76_77delinsGG	NP_000305.3:p.Thr26Gly
NM_000314.6:c.76_77delinsGG	NP_000305.3:p.Thr26Gly
NM_001304717.2:c.595_596delinsGG	NP_001291646.2:p.Thr199Gly
NM_001304718.1:c.-630_-629delinsGG	NP_001291647.1:n.-630_-629delinsGG
XM_006717926.2:c.76_77delinsGG	XP_006717989.1:p.Thr26Gly
XM_011539981.1:c.76_77delinsGG	XP_011538283.1:p.Thr26Gly
XR_945789.1:n.788_789delinsGG
XR_945790.1:n.788_789delinsGG
XR_945791.1:n.788_789delinsGG
NM_000314.7:c.76_77delinsGG	NP_000305.3:p.Thr26Gly
NM_001304717.5:c.595_596delinsGG	NP_001291646.4:p.Thr199Gly
NM_001304718.2:c.-630_-629delinsGG	NP_001291647.1:n.-630_-629delinsGG
NM_000314.8:c.76_77delinsGG MANE Select	NP_000305.3:p.Thr26Gly