Canonical Allele Identifier: CA645553956

Gene: PTEN

Linked Data

• COSMIC: COSM1173630

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957911_87957912insCACACAGC , CM000672.2:g.87957911_87957912insCACACAGC	GRCh38
NC_000010.10:g.89717668_89717669insCACACAGC , CM000672.1:g.89717668_89717669insCACACAGC	GRCh37
NC_000010.9:g.89707648_89707649insCACACAGC	NCBI36
NG_007466.2:g.99473_99474insCACACAGC , LRG_311:g.99473_99474insCACACAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.693_694insCACACAGC	ENSP00000514759.2:p.Thr232HisfsTer27
ENST00000710265.1:c.693_694insCACACAGC	ENSP00000518161.1:p.Thr232HisfsTer27
ENST00000472832.3:c.693_694insCACACAGC	ENSP00000483066.2:p.Thr232HisfsTer27
ENST00000688158.2:n.1428_1429insCACACAGC
ENST00000688922.2:c.*523_*524insCACACAGC	ENSP00000508742.2:n.*523_*524insCACACAGC
ENST00000700021.1:c.648_649insCACACAGC	ENSP00000514757.1:p.Thr217HisfsTer27
ENST00000700022.1:c.*32_*33insCACACAGC	ENSP00000514758.1:n.*32_*33insCACACAGC
ENST00000700023.1:n.1851_1852insCACACAGC
ENST00000700024.1:n.2085_2086insCACACAGC
ENST00000700025.1:n.1462_1463insCACACAGC
ENST00000700026.1:n.330_331insCACACAGC
ENST00000700029.1:c.527_528insCACACAGC
ENST00000706954.1:c.693_694insCACACAGC	ENSP00000516674.1:p.Thr232HisfsTer27
ENST00000706955.1:c.*728_*729insCACACAGC	ENSP00000516675.1:n.*728_*729insCACACAGC
ENST00000686459.1:c.*279_*280insCACACAGC	ENSP00000508909.1:n.*279_*280insCACACAGC
ENST00000688158.1:c.*804_*805insCACACAGC	ENSP00000509254.1:n.*804_*805insCACACAGC
ENST00000688308.1:c.693_694insCACACAGC	ENSP00000508752.1:p.Thr232HisfsTer27
ENST00000688922.1:c.614_615insCACACAGC
ENST00000693560.1:c.1212_1213insCACACAGC	ENSP00000509861.1:p.Thr405HisfsTer27
ENST00000371953.8:c.693_694insCACACAGC MANE Select	ENSP00000361021.3:p.Thr232HisfsTer27
ENST00000371953.7:c.693_694insCACACAGC	ENSP00000361021.3:p.Thr232HisfsTer27
ENST00000472832.2:c.120_121insCACACAGC	ENSP00000483066.1:p.Thr41HisfsTer27
NM_000314.5:c.693_694insCACACAGC	NP_000305.3:p.Thr232HisfsTer27
NM_000314.6:c.693_694insCACACAGC	NP_000305.3:p.Thr232HisfsTer27
NM_001304717.2:c.1212_1213insCACACAGC	NP_001291646.2:p.Thr405HisfsTer27
NM_001304718.1:c.102_103insCACACAGC	NP_001291647.1:p.Thr35HisfsTer27
XM_006717926.2:c.648_649insCACACAGC	XP_006717989.1:p.Thr217HisfsTer27
XM_011539981.1:c.693_694insCACACAGC	XP_011538283.1:p.Thr232HisfsTer27
XM_011539982.1:c.597_598insCACACAGC	XP_011538284.1:p.Thr200HisfsTer27
XR_945791.1:n.1263_1264insCACACAGC
NM_000314.7:c.693_694insCACACAGC	NP_000305.3:p.Thr232HisfsTer27
NM_001304717.5:c.1212_1213insCACACAGC	NP_001291646.4:p.Thr405HisfsTer27
NM_001304718.2:c.102_103insCACACAGC	NP_001291647.1:p.Thr35HisfsTer27
NM_000314.8:c.693_694insCACACAGC MANE Select	NP_000305.3:p.Thr232HisfsTer27