Canonical Allele Identifier: CA891838683

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952133_87952135delinsTGG , CM000672.2:g.87952133_87952135delinsTGG	GRCh38
NC_000010.10:g.89711890_89711892delinsTGG , CM000672.1:g.89711890_89711892delinsTGG	GRCh37
NC_000010.9:g.89701870_89701872delinsTGG	NCBI36
NG_007466.2:g.93695_93697delinsTGG , LRG_311:g.93695_93697delinsTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.508_510delinsTGG	ENSP00000514759.2:p.Ser170Trp
ENST00000710265.1:c.508_510delinsTGG	ENSP00000518161.1:p.Ser170Trp
ENST00000472832.3:c.508_510delinsTGG	ENSP00000483066.2:p.Ser170Trp
ENST00000688158.2:n.1243_1245delinsTGG
ENST00000688922.2:c.*338_*340delinsTGG	ENSP00000508742.2:n.*338_*340delinsTGG
ENST00000700021.1:c.463_465delinsTGG	ENSP00000514757.1:p.Ser155Trp
ENST00000700022.1:c.493-5720_493-5718delinsTGG	ENSP00000514758.1:n.493-5720_493-5718delinsTGG
ENST00000700023.1:n.1666_1668delinsTGG
ENST00000700024.1:n.1900_1902delinsTGG
ENST00000700025.1:n.1277_1279delinsTGG
ENST00000700029.1:c.342_344delinsTGG
ENST00000706954.1:c.508_510delinsTGG	ENSP00000516674.1:p.Ser170Trp
ENST00000706955.1:c.*543_*545delinsTGG	ENSP00000516675.1:n.*543_*545delinsTGG
ENST00000686459.1:c.*94_*96delinsTGG	ENSP00000508909.1:n.*94_*96delinsTGG
ENST00000688158.1:c.*619_*621delinsTGG	ENSP00000509254.1:n.*619_*621delinsTGG
ENST00000688308.1:c.508_510delinsTGG	ENSP00000508752.1:p.Ser170Trp
ENST00000688922.1:c.429_431delinsTGG
ENST00000693560.1:c.1027_1029delinsTGG	ENSP00000509861.1:p.Ser343Trp
ENST00000371953.8:c.508_510delinsTGG MANE Select	ENSP00000361021.3:p.Ser170Trp
ENST00000371953.7:c.508_510delinsTGG	ENSP00000361021.3:p.Ser170Trp
NM_000314.5:c.508_510delinsTGG	NP_000305.3:p.Ser170Trp
NM_000314.6:c.508_510delinsTGG	NP_000305.3:p.Ser170Trp
NM_001304717.2:c.1027_1029delinsTGG	NP_001291646.2:p.Ser343Trp
NM_001304718.1:c.-84_-82delinsTGG	NP_001291647.1:n.-84_-82delinsTGG
XM_006717926.2:c.463_465delinsTGG	XP_006717989.1:p.Ser155Trp
XM_011539981.1:c.508_510delinsTGG	XP_011538283.1:p.Ser170Trp
XM_011539982.1:c.412_414delinsTGG	XP_011538284.1:p.Ser138Trp
XR_945789.1:n.1379_1381delinsTGG
XR_945790.1:n.1496_1498delinsTGG
XR_945791.1:n.1205-5720_1205-5718delinsTGG
NM_000314.7:c.508_510delinsTGG	NP_000305.3:p.Ser170Trp
NM_001304717.5:c.1027_1029delinsTGG	NP_001291646.4:p.Ser343Trp
NM_001304718.2:c.-84_-82delinsTGG	NP_001291647.1:n.-84_-82delinsTGG
NM_000314.8:c.508_510delinsTGG MANE Select	NP_000305.3:p.Ser170Trp