Canonical Allele Identifier: CA1926175226

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87933145_87933146delinsGA , CM000672.2:g.87933145_87933146delinsGA	GRCh38
NC_000010.10:g.89692902_89692903delinsGA , CM000672.1:g.89692902_89692903delinsGA	GRCh37
NC_000010.9:g.89682882_89682883delinsGA	NCBI36
NG_007466.2:g.74707_74708delinsGA , LRG_311:g.74707_74708delinsGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.386_387delinsGA	ENSP00000514759.2:p.Gly129=
ENST00000710265.1:c.386_387delinsGA	ENSP00000518161.1:p.Gly129=
ENST00000472832.3:c.386_387delinsGA	ENSP00000483066.2:p.Gly129=
ENST00000688158.2:n.1121_1122delinsGA
ENST00000688922.2:c.*216_*217delinsGA	ENSP00000508742.2:n.*216_*217delinsGA
ENST00000700021.1:c.341_342delinsGA	ENSP00000514757.1:p.Gly114=
ENST00000700022.1:c.386_387delinsGA	ENSP00000514758.1:p.Gly129=
ENST00000700029.1:c.220_221delinsGA
ENST00000706954.1:c.386_387delinsGA	ENSP00000516674.1:p.Gly129=
ENST00000706955.1:c.*421_*422delinsGA	ENSP00000516675.1:n.*421_*422delinsGA
ENST00000686459.1:c.386_387delinsGA	ENSP00000508909.1:p.Gly129=
ENST00000688158.1:c.*497_*498delinsGA	ENSP00000509254.1:n.*497_*498delinsGA
ENST00000688308.1:c.386_387delinsGA	ENSP00000508752.1:p.Gly129=
ENST00000688922.1:c.307_308delinsGA
ENST00000693560.1:c.905_906delinsGA	ENSP00000509861.1:p.Gly302=
ENST00000371953.8:c.386_387delinsGA MANE Select	ENSP00000361021.3:p.Gly129=
ENST00000371953.7:c.386_387delinsGA	ENSP00000361021.3:p.Gly129=
ENST00000498703.1:n.212_213delinsGA
ENST00000610634.1:c.284_285delinsGA	ENSP00000477517.1:p.Gly95=
NM_000314.5:c.386_387delinsGA	NP_000305.3:p.Gly129=
NM_000314.6:c.386_387delinsGA	NP_000305.3:p.Gly129=
NM_001304717.2:c.905_906delinsGA	NP_001291646.2:p.Gly302=
NM_001304718.1:c.-365_-364delinsGA	NP_001291647.1:n.-365_-364delinsGA
XM_006717926.2:c.341_342delinsGA	XP_006717989.1:p.Gly114=
XM_011539981.1:c.386_387delinsGA	XP_011538283.1:p.Gly129=
XM_011539982.1:c.290_291delinsGA	XP_011538284.1:p.Gly97=
XR_945789.1:n.1098_1099delinsGA
XR_945790.1:n.1098_1099delinsGA
XR_945791.1:n.1098_1099delinsGA
NM_000314.7:c.386_387delinsGA	NP_000305.3:p.Gly129=
NM_001304717.5:c.905_906delinsGA	NP_001291646.4:p.Gly302=
NM_001304718.2:c.-365_-364delinsGA	NP_001291647.1:n.-365_-364delinsGA
NM_000314.8:c.386_387delinsGA MANE Select	NP_000305.3:p.Gly129=