Canonical Allele Identifier: CA891836298

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961026_87961028delinsTCT , CM000672.2:g.87961026_87961028delinsTCT	GRCh38
NC_000010.10:g.89720783_89720785delinsTCT , CM000672.1:g.89720783_89720785delinsTCT	GRCh37
NC_000010.9:g.89710763_89710765delinsTCT	NCBI36
NG_007466.2:g.102588_102590delinsTCT , LRG_311:g.102588_102590delinsTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1027_1029delinsTCT	ENSP00000514759.2:p.Asp343Ser
ENST00000710265.1:c.934_936delinsTCT	ENSP00000518161.1:p.Asp312Ser
ENST00000472832.3:c.934_936delinsTCT	ENSP00000483066.2:p.Asp312Ser
ENST00000688158.2:n.1669_1671delinsTCT
ENST00000688922.2:c.*764_*766delinsTCT	ENSP00000508742.2:n.*764_*766delinsTCT
ENST00000700021.1:c.889_891delinsTCT	ENSP00000514757.1:p.Asp297Ser
ENST00000700022.1:c.*273_*275delinsTCT	ENSP00000514758.1:n.*273_*275delinsTCT
ENST00000700023.1:n.2092_2094delinsTCT
ENST00000700024.1:n.2326_2328delinsTCT
ENST00000700025.1:n.1703_1705delinsTCT
ENST00000700026.1:n.571_573delinsTCT
ENST00000706954.1:c.934_936delinsTCT	ENSP00000516674.1:p.Asp312Ser
ENST00000706955.1:c.*969_*971delinsTCT	ENSP00000516675.1:n.*969_*971delinsTCT
ENST00000686459.1:c.*520_*522delinsTCT	ENSP00000508909.1:n.*520_*522delinsTCT
ENST00000688158.1:c.*1045_*1047delinsTCT	ENSP00000509254.1:n.*1045_*1047delinsTCT
ENST00000688308.1:c.934_936delinsTCT	ENSP00000508752.1:p.Asp312Ser
ENST00000688922.1:c.855_857delinsTCT
ENST00000693560.1:c.1453_1455delinsTCT	ENSP00000509861.1:p.Asp485Ser
ENST00000371953.8:c.934_936delinsTCT MANE Select	ENSP00000361021.3:p.Asp312Ser
ENST00000371953.7:c.934_936delinsTCT	ENSP00000361021.3:p.Asp312Ser
ENST00000472832.2:c.361_363delinsTCT	ENSP00000483066.1:p.Asp121Ser
NM_000314.5:c.934_936delinsTCT	NP_000305.3:p.Asp312Ser
NM_000314.6:c.934_936delinsTCT	NP_000305.3:p.Asp312Ser
NM_001304717.2:c.1453_1455delinsTCT	NP_001291646.2:p.Asp485Ser
NM_001304718.1:c.343_345delinsTCT	NP_001291647.1:p.Asp115Ser
XM_006717926.2:c.889_891delinsTCT	XP_006717989.1:p.Asp297Ser
XM_011539981.1:c.934_936delinsTCT	XP_011538283.1:p.Asp312Ser
XM_011539982.1:c.838_840delinsTCT	XP_011538284.1:p.Asp280Ser
XR_945791.1:n.1504_1506delinsTCT
NM_000314.7:c.934_936delinsTCT	NP_000305.3:p.Asp312Ser
NM_001304717.5:c.1453_1455delinsTCT	NP_001291646.4:p.Asp485Ser
NM_001304718.2:c.343_345delinsTCT	NP_001291647.1:p.Asp115Ser
NM_000314.8:c.934_936delinsTCT MANE Select	NP_000305.3:p.Asp312Ser