Canonical Allele Identifier: CA891834684

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87894051_87894053delinsTGT , CM000672.2:g.87894051_87894053delinsTGT	GRCh38
NC_000010.10:g.89653808_89653810delinsTGT , CM000672.1:g.89653808_89653810delinsTGT	GRCh37
NC_000010.9:g.89643788_89643790delinsTGT	NCBI36
NG_007466.2:g.35613_35615delinsTGT , LRG_311:g.35613_35615delinsTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.106_108delinsTGT	ENSP00000514759.2:p.Gly36Cys
ENST00000710265.1:c.106_108delinsTGT	ENSP00000518161.1:p.Gly36Cys
ENST00000472832.3:c.106_108delinsTGT	ENSP00000483066.2:p.Gly36Cys
ENST00000688158.2:n.899+13613_899+13615delinsTGT
ENST00000688922.2:c.106_108delinsTGT	ENSP00000508742.2:p.Gly36Cys
ENST00000700021.1:c.106_108delinsTGT	ENSP00000514757.1:p.Gly36Cys
ENST00000700022.1:c.106_108delinsTGT	ENSP00000514758.1:p.Gly36Cys
ENST00000706954.1:c.106_108delinsTGT	ENSP00000516674.1:p.Gly36Cys
ENST00000706955.1:c.*141_*143delinsTGT	ENSP00000516675.1:n.*141_*143delinsTGT
ENST00000686459.1:c.106_108delinsTGT	ENSP00000508909.1:p.Gly36Cys
ENST00000688158.1:c.*275+13613_*275+13615delinsTGT	ENSP00000509254.1:n.*275+13613_*275+13615delinsTGT
ENST00000688308.1:c.106_108delinsTGT	ENSP00000508752.1:p.Gly36Cys
ENST00000693560.1:c.625_627delinsTGT	ENSP00000509861.1:p.Gly209Cys
ENST00000371953.8:c.106_108delinsTGT MANE Select	ENSP00000361021.3:p.Gly36Cys
ENST00000371953.7:c.106_108delinsTGT	ENSP00000361021.3:p.Gly36Cys
ENST00000462694.1:n.108_110delinsTGT
ENST00000610634.1:c.4_6delinsTGT	ENSP00000477517.1:p.Gly2Cys
NM_000314.5:c.106_108delinsTGT	NP_000305.3:p.Gly36Cys
NM_000314.6:c.106_108delinsTGT	NP_000305.3:p.Gly36Cys
NM_001304717.2:c.625_627delinsTGT	NP_001291646.2:p.Gly209Cys
NM_001304718.1:c.-600_-598delinsTGT	NP_001291647.1:n.-600_-598delinsTGT
XM_006717926.2:c.106_108delinsTGT	XP_006717989.1:p.Gly36Cys
XM_011539981.1:c.106_108delinsTGT	XP_011538283.1:p.Gly36Cys
XM_011539982.1:c.68+13613_68+13615delinsTGT	XP_011538284.1:n.68+13613_68+13615delinsTGT
XR_945789.1:n.818_820delinsTGT
XR_945790.1:n.818_820delinsTGT
XR_945791.1:n.818_820delinsTGT
NM_000314.7:c.106_108delinsTGT	NP_000305.3:p.Gly36Cys
NM_001304717.5:c.625_627delinsTGT	NP_001291646.4:p.Gly209Cys
NM_001304718.2:c.-600_-598delinsTGT	NP_001291647.1:n.-600_-598delinsTGT
NM_000314.8:c.106_108delinsTGT MANE Select	NP_000305.3:p.Gly36Cys