Canonical Allele Identifier: CA2579926724

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960955_87960956delinsGT , CM000672.2:g.87960955_87960956delinsGT	GRCh38
NC_000010.10:g.89720712_89720713delinsGT , CM000672.1:g.89720712_89720713delinsGT	GRCh37
NC_000010.9:g.89710692_89710693delinsGT	NCBI36
NG_007466.2:g.102517_102518delinsGT , LRG_311:g.102517_102518delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.956_957delinsGT	ENSP00000514759.2:p.Glu319Gly
ENST00000710265.1:c.863_864delinsGT	ENSP00000518161.1:p.Glu288Gly
ENST00000472832.3:c.863_864delinsGT	ENSP00000483066.2:p.Glu288Gly
ENST00000688158.2:n.1598_1599delinsGT
ENST00000688922.2:c.*693_*694delinsGT	ENSP00000508742.2:n.*693_*694delinsGT
ENST00000700021.1:c.818_819delinsGT	ENSP00000514757.1:p.Glu273Gly
ENST00000700022.1:c.*202_*203delinsGT	ENSP00000514758.1:n.*202_*203delinsGT
ENST00000700023.1:n.2021_2022delinsGT
ENST00000700024.1:n.2255_2256delinsGT
ENST00000700025.1:n.1632_1633delinsGT
ENST00000700026.1:n.500_501delinsGT
ENST00000700029.1:c.790_791delinsGT
ENST00000706954.1:c.863_864delinsGT	ENSP00000516674.1:p.Glu288Gly
ENST00000706955.1:c.*898_*899delinsGT	ENSP00000516675.1:n.*898_*899delinsGT
ENST00000686459.1:c.*449_*450delinsGT	ENSP00000508909.1:n.*449_*450delinsGT
ENST00000688158.1:c.*974_*975delinsGT	ENSP00000509254.1:n.*974_*975delinsGT
ENST00000688308.1:c.863_864delinsGT	ENSP00000508752.1:p.Glu288Gly
ENST00000688922.1:c.784_785delinsGT
ENST00000693560.1:c.1382_1383delinsGT	ENSP00000509861.1:p.Glu461Gly
ENST00000371953.8:c.863_864delinsGT MANE Select	ENSP00000361021.3:p.Glu288Gly
ENST00000371953.7:c.863_864delinsGT	ENSP00000361021.3:p.Glu288Gly
ENST00000472832.2:c.290_291delinsGT	ENSP00000483066.1:p.Glu97Gly
NM_000314.5:c.863_864delinsGT	NP_000305.3:p.Glu288Gly
NM_000314.6:c.863_864delinsGT	NP_000305.3:p.Glu288Gly
NM_001304717.2:c.1382_1383delinsGT	NP_001291646.2:p.Glu461Gly
NM_001304718.1:c.272_273delinsGT	NP_001291647.1:p.Glu91Gly
XM_006717926.2:c.818_819delinsGT	XP_006717989.1:p.Glu273Gly
XM_011539981.1:c.863_864delinsGT	XP_011538283.1:p.Glu288Gly
XM_011539982.1:c.767_768delinsGT	XP_011538284.1:p.Glu256Gly
XR_945791.1:n.1433_1434delinsGT
NM_000314.7:c.863_864delinsGT	NP_000305.3:p.Glu288Gly
NM_001304717.5:c.1382_1383delinsGT	NP_001291646.4:p.Glu461Gly
NM_001304718.2:c.272_273delinsGT	NP_001291647.1:p.Glu91Gly
NM_000314.8:c.863_864delinsGT MANE Select	NP_000305.3:p.Glu288Gly