Canonical Allele Identifier: CA891838681

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952133_87952135delinsCCA , CM000672.2:g.87952133_87952135delinsCCA	GRCh38
NC_000010.10:g.89711890_89711892delinsCCA , CM000672.1:g.89711890_89711892delinsCCA	GRCh37
NC_000010.9:g.89701870_89701872delinsCCA	NCBI36
NG_007466.2:g.93695_93697delinsCCA , LRG_311:g.93695_93697delinsCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.508_510delinsCCA	ENSP00000514759.2:p.Ser170Pro
ENST00000710265.1:c.508_510delinsCCA	ENSP00000518161.1:p.Ser170Pro
ENST00000472832.3:c.508_510delinsCCA	ENSP00000483066.2:p.Ser170Pro
ENST00000688158.2:n.1243_1245delinsCCA
ENST00000688922.2:c.*338_*340delinsCCA	ENSP00000508742.2:n.*338_*340delinsCCA
ENST00000700021.1:c.463_465delinsCCA	ENSP00000514757.1:p.Ser155Pro
ENST00000700022.1:c.493-5720_493-5718delinsCCA	ENSP00000514758.1:n.493-5720_493-5718delinsCCA
ENST00000700023.1:n.1666_1668delinsCCA
ENST00000700024.1:n.1900_1902delinsCCA
ENST00000700025.1:n.1277_1279delinsCCA
ENST00000700029.1:c.342_344delinsCCA
ENST00000706954.1:c.508_510delinsCCA	ENSP00000516674.1:p.Ser170Pro
ENST00000706955.1:c.*543_*545delinsCCA	ENSP00000516675.1:n.*543_*545delinsCCA
ENST00000686459.1:c.*94_*96delinsCCA	ENSP00000508909.1:n.*94_*96delinsCCA
ENST00000688158.1:c.*619_*621delinsCCA	ENSP00000509254.1:n.*619_*621delinsCCA
ENST00000688308.1:c.508_510delinsCCA	ENSP00000508752.1:p.Ser170Pro
ENST00000688922.1:c.429_431delinsCCA
ENST00000693560.1:c.1027_1029delinsCCA	ENSP00000509861.1:p.Ser343Pro
ENST00000371953.8:c.508_510delinsCCA MANE Select	ENSP00000361021.3:p.Ser170Pro
ENST00000371953.7:c.508_510delinsCCA	ENSP00000361021.3:p.Ser170Pro
NM_000314.5:c.508_510delinsCCA	NP_000305.3:p.Ser170Pro
NM_000314.6:c.508_510delinsCCA	NP_000305.3:p.Ser170Pro
NM_001304717.2:c.1027_1029delinsCCA	NP_001291646.2:p.Ser343Pro
NM_001304718.1:c.-84_-82delinsCCA	NP_001291647.1:n.-84_-82delinsCCA
XM_006717926.2:c.463_465delinsCCA	XP_006717989.1:p.Ser155Pro
XM_011539981.1:c.508_510delinsCCA	XP_011538283.1:p.Ser170Pro
XM_011539982.1:c.412_414delinsCCA	XP_011538284.1:p.Ser138Pro
XR_945789.1:n.1379_1381delinsCCA
XR_945790.1:n.1496_1498delinsCCA
XR_945791.1:n.1205-5720_1205-5718delinsCCA
NM_000314.7:c.508_510delinsCCA	NP_000305.3:p.Ser170Pro
NM_001304717.5:c.1027_1029delinsCCA	NP_001291646.4:p.Ser343Pro
NM_001304718.2:c.-84_-82delinsCCA	NP_001291647.1:n.-84_-82delinsCCA
NM_000314.8:c.508_510delinsCCA MANE Select	NP_000305.3:p.Ser170Pro