Canonical Allele Identifier: CA891838734

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952142_87952144delinsTGG , CM000672.2:g.87952142_87952144delinsTGG	GRCh38
NC_000010.10:g.89711899_89711901delinsTGG , CM000672.1:g.89711899_89711901delinsTGG	GRCh37
NC_000010.9:g.89701879_89701881delinsTGG	NCBI36
NG_007466.2:g.93704_93706delinsTGG , LRG_311:g.93704_93706delinsTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.517_519delinsTGG	ENSP00000514759.2:p.Arg173Trp
ENST00000710265.1:c.517_519delinsTGG	ENSP00000518161.1:p.Arg173Trp
ENST00000472832.3:c.517_519delinsTGG	ENSP00000483066.2:p.Arg173Trp
ENST00000688158.2:n.1252_1254delinsTGG
ENST00000688922.2:c.*347_*349delinsTGG	ENSP00000508742.2:n.*347_*349delinsTGG
ENST00000700021.1:c.472_474delinsTGG	ENSP00000514757.1:p.Arg158Trp
ENST00000700022.1:c.493-5711_493-5709delinsTGG	ENSP00000514758.1:n.493-5711_493-5709delinsTGG
ENST00000700023.1:n.1675_1677delinsTGG
ENST00000700024.1:n.1909_1911delinsTGG
ENST00000700025.1:n.1286_1288delinsTGG
ENST00000700029.1:c.351_353delinsTGG
ENST00000706954.1:c.517_519delinsTGG	ENSP00000516674.1:p.Arg173Trp
ENST00000706955.1:c.*552_*554delinsTGG	ENSP00000516675.1:n.*552_*554delinsTGG
ENST00000686459.1:c.*103_*105delinsTGG	ENSP00000508909.1:n.*103_*105delinsTGG
ENST00000688158.1:c.*628_*630delinsTGG	ENSP00000509254.1:n.*628_*630delinsTGG
ENST00000688308.1:c.517_519delinsTGG	ENSP00000508752.1:p.Arg173Trp
ENST00000688922.1:c.438_440delinsTGG
ENST00000693560.1:c.1036_1038delinsTGG	ENSP00000509861.1:p.Arg346Trp
ENST00000371953.8:c.517_519delinsTGG MANE Select	ENSP00000361021.3:p.Arg173Trp
ENST00000371953.7:c.517_519delinsTGG	ENSP00000361021.3:p.Arg173Trp
NM_000314.5:c.517_519delinsTGG	NP_000305.3:p.Arg173Trp
NM_000314.6:c.517_519delinsTGG	NP_000305.3:p.Arg173Trp
NM_001304717.2:c.1036_1038delinsTGG	NP_001291646.2:p.Arg346Trp
NM_001304718.1:c.-75_-73delinsTGG	NP_001291647.1:n.-75_-73delinsTGG
XM_006717926.2:c.472_474delinsTGG	XP_006717989.1:p.Arg158Trp
XM_011539981.1:c.517_519delinsTGG	XP_011538283.1:p.Arg173Trp
XM_011539982.1:c.421_423delinsTGG	XP_011538284.1:p.Arg141Trp
XR_945789.1:n.1388_1390delinsTGG
XR_945790.1:n.1505_1507delinsTGG
XR_945791.1:n.1205-5711_1205-5709delinsTGG
NM_000314.7:c.517_519delinsTGG	NP_000305.3:p.Arg173Trp
NM_001304717.5:c.1036_1038delinsTGG	NP_001291646.4:p.Arg346Trp
NM_001304718.2:c.-75_-73delinsTGG	NP_001291647.1:n.-75_-73delinsTGG
NM_000314.8:c.517_519delinsTGG MANE Select	NP_000305.3:p.Arg173Trp