Canonical Allele Identifier: CA891836863

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961080_87961082delinsTCT , CM000672.2:g.87961080_87961082delinsTCT	GRCh38
NC_000010.10:g.89720837_89720839delinsTCT , CM000672.1:g.89720837_89720839delinsTCT	GRCh37
NC_000010.9:g.89710817_89710819delinsTCT	NCBI36
NG_007466.2:g.102642_102644delinsTCT , LRG_311:g.102642_102644delinsTCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.1081_1083delinsTCT	ENSP00000514759.2:p.Lys361Ser
ENST00000710265.1:c.988_990delinsTCT	ENSP00000518161.1:p.Lys330Ser
ENST00000472832.3:c.988_990delinsTCT	ENSP00000483066.2:p.Lys330Ser
ENST00000688158.2:n.1723_1725delinsTCT
ENST00000688922.2:c.*818_*820delinsTCT	ENSP00000508742.2:n.*818_*820delinsTCT
ENST00000700021.1:c.943_945delinsTCT	ENSP00000514757.1:p.Lys315Ser
ENST00000700022.1:c.*327_*329delinsTCT	ENSP00000514758.1:n.*327_*329delinsTCT
ENST00000700023.1:n.2146_2148delinsTCT
ENST00000700024.1:n.2380_2382delinsTCT
ENST00000700025.1:n.1757_1759delinsTCT
ENST00000700026.1:n.625_627delinsTCT
ENST00000706954.1:c.988_990delinsTCT	ENSP00000516674.1:p.Lys330Ser
ENST00000706955.1:c.*1023_*1025delinsTCT	ENSP00000516675.1:n.*1023_*1025delinsTCT
ENST00000686459.1:c.*574_*576delinsTCT	ENSP00000508909.1:n.*574_*576delinsTCT
ENST00000688158.1:c.*1099_*1101delinsTCT	ENSP00000509254.1:n.*1099_*1101delinsTCT
ENST00000688308.1:c.988_990delinsTCT	ENSP00000508752.1:p.Lys330Ser
ENST00000688922.1:c.909_911delinsTCT
ENST00000693560.1:c.1507_1509delinsTCT	ENSP00000509861.1:p.Lys503Ser
ENST00000371953.8:c.988_990delinsTCT MANE Select	ENSP00000361021.3:p.Lys330Ser
ENST00000371953.7:c.988_990delinsTCT	ENSP00000361021.3:p.Lys330Ser
ENST00000472832.2:c.415_417delinsTCT	ENSP00000483066.1:p.Lys139Ser
NM_000314.5:c.988_990delinsTCT	NP_000305.3:p.Lys330Ser
NM_000314.6:c.988_990delinsTCT	NP_000305.3:p.Lys330Ser
NM_001304717.2:c.1507_1509delinsTCT	NP_001291646.2:p.Lys503Ser
NM_001304718.1:c.397_399delinsTCT	NP_001291647.1:p.Lys133Ser
XM_006717926.2:c.943_945delinsTCT	XP_006717989.1:p.Lys315Ser
XM_011539981.1:c.988_990delinsTCT	XP_011538283.1:p.Lys330Ser
XM_011539982.1:c.892_894delinsTCT	XP_011538284.1:p.Lys298Ser
XR_945791.1:n.1558_1560delinsTCT
NM_000314.7:c.988_990delinsTCT	NP_000305.3:p.Lys330Ser
NM_001304717.5:c.1507_1509delinsTCT	NP_001291646.4:p.Lys503Ser
NM_001304718.2:c.397_399delinsTCT	NP_001291647.1:p.Lys133Ser
NM_000314.8:c.988_990delinsTCT MANE Select	NP_000305.3:p.Lys330Ser