Canonical Allele Identifier: CA891840998

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960903_87960904delinsGG , CM000672.2:g.87960903_87960904delinsGG	GRCh38
NC_000010.10:g.89720660_89720661delinsGG , CM000672.1:g.89720660_89720661delinsGG	GRCh37
NC_000010.9:g.89710640_89710641delinsGG	NCBI36
NG_007466.2:g.102465_102466delinsGG , LRG_311:g.102465_102466delinsGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.904_905delinsGG	ENSP00000514759.2:p.Phe302Gly
ENST00000710265.1:c.811_812delinsGG	ENSP00000518161.1:p.Phe271Gly
ENST00000472832.3:c.811_812delinsGG	ENSP00000483066.2:p.Phe271Gly
ENST00000688158.2:n.1546_1547delinsGG
ENST00000688922.2:c.*641_*642delinsGG	ENSP00000508742.2:n.*641_*642delinsGG
ENST00000700021.1:c.766_767delinsGG	ENSP00000514757.1:p.Phe256Gly
ENST00000700022.1:c.*150_*151delinsGG	ENSP00000514758.1:n.*150_*151delinsGG
ENST00000700023.1:n.1969_1970delinsGG
ENST00000700024.1:n.2203_2204delinsGG
ENST00000700025.1:n.1580_1581delinsGG
ENST00000700026.1:n.448_449delinsGG
ENST00000700029.1:c.738_739delinsGG
ENST00000706954.1:c.811_812delinsGG	ENSP00000516674.1:p.Phe271Gly
ENST00000706955.1:c.*846_*847delinsGG	ENSP00000516675.1:n.*846_*847delinsGG
ENST00000686459.1:c.*397_*398delinsGG	ENSP00000508909.1:n.*397_*398delinsGG
ENST00000688158.1:c.*922_*923delinsGG	ENSP00000509254.1:n.*922_*923delinsGG
ENST00000688308.1:c.811_812delinsGG	ENSP00000508752.1:p.Phe271Gly
ENST00000688922.1:c.732_733delinsGG
ENST00000693560.1:c.1330_1331delinsGG	ENSP00000509861.1:p.Phe444Gly
ENST00000371953.8:c.811_812delinsGG MANE Select	ENSP00000361021.3:p.Phe271Gly
ENST00000371953.7:c.811_812delinsGG	ENSP00000361021.3:p.Phe271Gly
ENST00000472832.2:c.238_239delinsGG	ENSP00000483066.1:p.Phe80Gly
NM_000314.5:c.811_812delinsGG	NP_000305.3:p.Phe271Gly
NM_000314.6:c.811_812delinsGG	NP_000305.3:p.Phe271Gly
NM_001304717.2:c.1330_1331delinsGG	NP_001291646.2:p.Phe444Gly
NM_001304718.1:c.220_221delinsGG	NP_001291647.1:p.Phe74Gly
XM_006717926.2:c.766_767delinsGG	XP_006717989.1:p.Phe256Gly
XM_011539981.1:c.811_812delinsGG	XP_011538283.1:p.Phe271Gly
XM_011539982.1:c.715_716delinsGG	XP_011538284.1:p.Phe239Gly
XR_945791.1:n.1381_1382delinsGG
NM_000314.7:c.811_812delinsGG	NP_000305.3:p.Phe271Gly
NM_001304717.5:c.1330_1331delinsGG	NP_001291646.4:p.Phe444Gly
NM_001304718.2:c.220_221delinsGG	NP_001291647.1:p.Phe74Gly
NM_000314.8:c.811_812delinsGG MANE Select	NP_000305.3:p.Phe271Gly