Canonical Allele Identifier: CA891838767

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952149_87952150delinsCT , CM000672.2:g.87952149_87952150delinsCT	GRCh38
NC_000010.10:g.89711906_89711907delinsCT , CM000672.1:g.89711906_89711907delinsCT	GRCh37
NC_000010.9:g.89701886_89701887delinsCT	NCBI36
NG_007466.2:g.93711_93712delinsCT , LRG_311:g.93711_93712delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.524_525delinsCT	ENSP00000514759.2:p.Val175Ala
ENST00000710265.1:c.524_525delinsCT	ENSP00000518161.1:p.Val175Ala
ENST00000472832.3:c.524_525delinsCT	ENSP00000483066.2:p.Val175Ala
ENST00000688158.2:n.1259_1260delinsCT
ENST00000688922.2:c.*354_*355delinsCT	ENSP00000508742.2:n.*354_*355delinsCT
ENST00000700021.1:c.479_480delinsCT	ENSP00000514757.1:p.Val160Ala
ENST00000700022.1:c.493-5704_493-5703delinsCT	ENSP00000514758.1:n.493-5704_493-5703delinsCT
ENST00000700023.1:n.1682_1683delinsCT
ENST00000700024.1:n.1916_1917delinsCT
ENST00000700025.1:n.1293_1294delinsCT
ENST00000700029.1:c.358_359delinsCT
ENST00000706954.1:c.524_525delinsCT	ENSP00000516674.1:p.Val175Ala
ENST00000706955.1:c.*559_*560delinsCT	ENSP00000516675.1:n.*559_*560delinsCT
ENST00000686459.1:c.*110_*111delinsCT	ENSP00000508909.1:n.*110_*111delinsCT
ENST00000688158.1:c.*635_*636delinsCT	ENSP00000509254.1:n.*635_*636delinsCT
ENST00000688308.1:c.524_525delinsCT	ENSP00000508752.1:p.Val175Ala
ENST00000688922.1:c.445_446delinsCT
ENST00000693560.1:c.1043_1044delinsCT	ENSP00000509861.1:p.Val348Ala
ENST00000371953.8:c.524_525delinsCT MANE Select	ENSP00000361021.3:p.Val175Ala
ENST00000371953.7:c.524_525delinsCT	ENSP00000361021.3:p.Val175Ala
NM_000314.5:c.524_525delinsCT	NP_000305.3:p.Val175Ala
NM_000314.6:c.524_525delinsCT	NP_000305.3:p.Val175Ala
NM_001304717.2:c.1043_1044delinsCT	NP_001291646.2:p.Val348Ala
NM_001304718.1:c.-68_-67delinsCT	NP_001291647.1:n.-68_-67delinsCT
XM_006717926.2:c.479_480delinsCT	XP_006717989.1:p.Val160Ala
XM_011539981.1:c.524_525delinsCT	XP_011538283.1:p.Val175Ala
XM_011539982.1:c.428_429delinsCT	XP_011538284.1:p.Val143Ala
XR_945789.1:n.1395_1396delinsCT
XR_945790.1:n.1512_1513delinsCT
XR_945791.1:n.1205-5704_1205-5703delinsCT
NM_000314.7:c.524_525delinsCT	NP_000305.3:p.Val175Ala
NM_001304717.5:c.1043_1044delinsCT	NP_001291646.4:p.Val348Ala
NM_001304718.2:c.-68_-67delinsCT	NP_001291647.1:n.-68_-67delinsCT
NM_000314.8:c.524_525delinsCT MANE Select	NP_000305.3:p.Val175Ala