Canonical Allele Identifier: CA2579926642

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961092_87961094delinsGCT , CM000672.2:g.87961092_87961094delinsGCT	GRCh38
NC_000010.10:g.89720849_89720851delinsGCT , CM000672.1:g.89720849_89720851delinsGCT	GRCh37
NC_000010.9:g.89710829_89710831delinsGCT	NCBI36
NG_007466.2:g.102654_102656delinsGCT , LRG_311:g.102654_102656delinsGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1093_1095delinsGCT	ENSP00000514759.2:p.Asn365Ala
ENST00000710265.1:c.1000_1002delinsGCT	ENSP00000518161.1:p.Asn334Ala
ENST00000472832.3:c.1000_1002delinsGCT	ENSP00000483066.2:p.Asn334Ala
ENST00000688158.2:n.1735_1737delinsGCT
ENST00000688922.2:c.*830_*832delinsGCT	ENSP00000508742.2:n.*830_*832delinsGCT
ENST00000700021.1:c.955_957delinsGCT	ENSP00000514757.1:p.Asn319Ala
ENST00000700022.1:c.*339_*341delinsGCT	ENSP00000514758.1:n.*339_*341delinsGCT
ENST00000700023.1:n.2158_2160delinsGCT
ENST00000700024.1:n.2392_2394delinsGCT
ENST00000700025.1:n.1769_1771delinsGCT
ENST00000700026.1:n.637_639delinsGCT
ENST00000706954.1:c.1000_1002delinsGCT	ENSP00000516674.1:p.Asn334Ala
ENST00000706955.1:c.*1035_*1037delinsGCT	ENSP00000516675.1:n.*1035_*1037delinsGCT
ENST00000686459.1:c.*586_*588delinsGCT	ENSP00000508909.1:n.*586_*588delinsGCT
ENST00000688158.1:c.*1111_*1113delinsGCT	ENSP00000509254.1:n.*1111_*1113delinsGCT
ENST00000688308.1:c.1000_1002delinsGCT	ENSP00000508752.1:p.Asn334Ala
ENST00000688922.1:c.921_923delinsGCT
ENST00000693560.1:c.1519_1521delinsGCT	ENSP00000509861.1:p.Asn507Ala
ENST00000371953.8:c.1000_1002delinsGCT MANE Select	ENSP00000361021.3:p.Asn334Ala
ENST00000371953.7:c.1000_1002delinsGCT	ENSP00000361021.3:p.Asn334Ala
ENST00000472832.2:c.427_429delinsGCT	ENSP00000483066.1:p.Asn143Ala
NM_000314.5:c.1000_1002delinsGCT	NP_000305.3:p.Asn334Ala
NM_000314.6:c.1000_1002delinsGCT	NP_000305.3:p.Asn334Ala
NM_001304717.2:c.1519_1521delinsGCT	NP_001291646.2:p.Asn507Ala
NM_001304718.1:c.409_411delinsGCT	NP_001291647.1:p.Asn137Ala
XM_006717926.2:c.955_957delinsGCT	XP_006717989.1:p.Asn319Ala
XM_011539981.1:c.1000_1002delinsGCT	XP_011538283.1:p.Asn334Ala
XM_011539982.1:c.904_906delinsGCT	XP_011538284.1:p.Asn302Ala
XR_945791.1:n.1570_1572delinsGCT
NM_000314.7:c.1000_1002delinsGCT	NP_000305.3:p.Asn334Ala
NM_001304717.5:c.1519_1521delinsGCT	NP_001291646.4:p.Asn507Ala
NM_001304718.2:c.409_411delinsGCT	NP_001291647.1:p.Asn137Ala
NM_000314.8:c.1000_1002delinsGCT MANE Select	NP_000305.3:p.Asn334Ala