Canonical Allele Identifier: CA891836871

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961081_87961082delinsCT , CM000672.2:g.87961081_87961082delinsCT	GRCh38
NC_000010.10:g.89720838_89720839delinsCT , CM000672.1:g.89720838_89720839delinsCT	GRCh37
NC_000010.9:g.89710818_89710819delinsCT	NCBI36
NG_007466.2:g.102643_102644delinsCT , LRG_311:g.102643_102644delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1082_1083delinsCT	ENSP00000514759.2:p.Lys361Thr
ENST00000710265.1:c.989_990delinsCT	ENSP00000518161.1:p.Lys330Thr
ENST00000472832.3:c.989_990delinsCT	ENSP00000483066.2:p.Lys330Thr
ENST00000688158.2:n.1724_1725delinsCT
ENST00000688922.2:c.*819_*820delinsCT	ENSP00000508742.2:n.*819_*820delinsCT
ENST00000700021.1:c.944_945delinsCT	ENSP00000514757.1:p.Lys315Thr
ENST00000700022.1:c.*328_*329delinsCT	ENSP00000514758.1:n.*328_*329delinsCT
ENST00000700023.1:n.2147_2148delinsCT
ENST00000700024.1:n.2381_2382delinsCT
ENST00000700025.1:n.1758_1759delinsCT
ENST00000700026.1:n.626_627delinsCT
ENST00000706954.1:c.989_990delinsCT	ENSP00000516674.1:p.Lys330Thr
ENST00000706955.1:c.*1024_*1025delinsCT	ENSP00000516675.1:n.*1024_*1025delinsCT
ENST00000686459.1:c.*575_*576delinsCT	ENSP00000508909.1:n.*575_*576delinsCT
ENST00000688158.1:c.*1100_*1101delinsCT	ENSP00000509254.1:n.*1100_*1101delinsCT
ENST00000688308.1:c.989_990delinsCT	ENSP00000508752.1:p.Lys330Thr
ENST00000688922.1:c.910_911delinsCT
ENST00000693560.1:c.1508_1509delinsCT	ENSP00000509861.1:p.Lys503Thr
ENST00000371953.8:c.989_990delinsCT MANE Select	ENSP00000361021.3:p.Lys330Thr
ENST00000371953.7:c.989_990delinsCT	ENSP00000361021.3:p.Lys330Thr
ENST00000472832.2:c.416_417delinsCT	ENSP00000483066.1:p.Lys139Thr
NM_000314.5:c.989_990delinsCT	NP_000305.3:p.Lys330Thr
NM_000314.6:c.989_990delinsCT	NP_000305.3:p.Lys330Thr
NM_001304717.2:c.1508_1509delinsCT	NP_001291646.2:p.Lys503Thr
NM_001304718.1:c.398_399delinsCT	NP_001291647.1:p.Lys133Thr
XM_006717926.2:c.944_945delinsCT	XP_006717989.1:p.Lys315Thr
XM_011539981.1:c.989_990delinsCT	XP_011538283.1:p.Lys330Thr
XM_011539982.1:c.893_894delinsCT	XP_011538284.1:p.Lys298Thr
XR_945791.1:n.1559_1560delinsCT
NM_000314.7:c.989_990delinsCT	NP_000305.3:p.Lys330Thr
NM_001304717.5:c.1508_1509delinsCT	NP_001291646.4:p.Lys503Thr
NM_001304718.2:c.398_399delinsCT	NP_001291647.1:p.Lys133Thr
NM_000314.8:c.989_990delinsCT MANE Select	NP_000305.3:p.Lys330Thr