Canonical Allele Identifier: CA891834718

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87894052_87894053delinsTT , CM000672.2:g.87894052_87894053delinsTT	GRCh38
NC_000010.10:g.89653809_89653810delinsTT , CM000672.1:g.89653809_89653810delinsTT	GRCh37
NC_000010.9:g.89643789_89643790delinsTT	NCBI36
NG_007466.2:g.35614_35615delinsTT , LRG_311:g.35614_35615delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.107_108delinsTT	ENSP00000514759.2:p.Gly36Val
ENST00000710265.1:c.107_108delinsTT	ENSP00000518161.1:p.Gly36Val
ENST00000472832.3:c.107_108delinsTT	ENSP00000483066.2:p.Gly36Val
ENST00000688158.2:n.899+13614_899+13615delinsTT
ENST00000688922.2:c.107_108delinsTT	ENSP00000508742.2:p.Gly36Val
ENST00000700021.1:c.107_108delinsTT	ENSP00000514757.1:p.Gly36Val
ENST00000700022.1:c.107_108delinsTT	ENSP00000514758.1:p.Gly36Val
ENST00000706954.1:c.107_108delinsTT	ENSP00000516674.1:p.Gly36Val
ENST00000706955.1:c.*142_*143delinsTT	ENSP00000516675.1:n.*142_*143delinsTT
ENST00000686459.1:c.107_108delinsTT	ENSP00000508909.1:p.Gly36Val
ENST00000688158.1:c.*275+13614_*275+13615delinsTT	ENSP00000509254.1:n.*275+13614_*275+13615delinsTT
ENST00000688308.1:c.107_108delinsTT	ENSP00000508752.1:p.Gly36Val
ENST00000693560.1:c.626_627delinsTT	ENSP00000509861.1:p.Gly209Val
ENST00000371953.8:c.107_108delinsTT MANE Select	ENSP00000361021.3:p.Gly36Val
ENST00000371953.7:c.107_108delinsTT	ENSP00000361021.3:p.Gly36Val
ENST00000462694.1:n.109_110delinsTT
ENST00000610634.1:c.5_6delinsTT	ENSP00000477517.1:p.Gly2Val
NM_000314.5:c.107_108delinsTT	NP_000305.3:p.Gly36Val
NM_000314.6:c.107_108delinsTT	NP_000305.3:p.Gly36Val
NM_001304717.2:c.626_627delinsTT	NP_001291646.2:p.Gly209Val
NM_001304718.1:c.-599_-598delinsTT	NP_001291647.1:n.-599_-598delinsTT
XM_006717926.2:c.107_108delinsTT	XP_006717989.1:p.Gly36Val
XM_011539981.1:c.107_108delinsTT	XP_011538283.1:p.Gly36Val
XM_011539982.1:c.68+13614_68+13615delinsTT	XP_011538284.1:n.68+13614_68+13615delinsTT
XR_945789.1:n.819_820delinsTT
XR_945790.1:n.819_820delinsTT
XR_945791.1:n.819_820delinsTT
NM_000314.7:c.107_108delinsTT	NP_000305.3:p.Gly36Val
NM_001304717.5:c.626_627delinsTT	NP_001291646.4:p.Gly209Val
NM_001304718.2:c.-599_-598delinsTT	NP_001291647.1:n.-599_-598delinsTT
NM_000314.8:c.107_108delinsTT MANE Select	NP_000305.3:p.Gly36Val