Canonical Allele Identifier: CA1926190008

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960975_87960992delinsCTATGTGATCAAGAAATC , CM000672.2:g.87960975_87960992delinsCTATGTGATCAAGAAATC	GRCh38
NC_000010.10:g.89720732_89720749delinsCTATGTGATCAAGAAATC , CM000672.1:g.89720732_89720749delinsCTATGTGATCAAGAAATC	GRCh37
NC_000010.9:g.89710712_89710729delinsCTATGTGATCAAGAAATC	NCBI36
NG_007466.2:g.102537_102554delinsCTATGTGATCAAGAAATC , LRG_311:g.102537_102554delinsCTATGTGATCAAGAAATC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.976_993delinsCTATGTGATCAAGAAATC	ENSP00000514759.2:p.Leu326=
ENST00000710265.1:c.883_900delinsCTATGTGATCAAGAAATC	ENSP00000518161.1:p.Leu295=
ENST00000472832.3:c.883_900delinsCTATGTGATCAAGAAATC	ENSP00000483066.2:p.Leu295=
ENST00000688158.2:n.1618_1635delinsCTATGTGATCAAGAAATC
ENST00000688922.2:c.*713_*730delinsCTATGTGATCAAGAAATC	ENSP00000508742.2:n.*713_*730delinsCTATGTGATCAAGAAATC
ENST00000700021.1:c.838_855delinsCTATGTGATCAAGAAATC	ENSP00000514757.1:p.Leu280=
ENST00000700022.1:c.*222_*239delinsCTATGTGATCAAGAAATC	ENSP00000514758.1:n.*222_*239delinsCTATGTGATCAAGAAATC
ENST00000700023.1:n.2041_2058delinsCTATGTGATCAAGAAATC
ENST00000700024.1:n.2275_2292delinsCTATGTGATCAAGAAATC
ENST00000700025.1:n.1652_1669delinsCTATGTGATCAAGAAATC
ENST00000700026.1:n.520_537delinsCTATGTGATCAAGAAATC
ENST00000706954.1:c.883_900delinsCTATGTGATCAAGAAATC	ENSP00000516674.1:p.Leu295=
ENST00000706955.1:c.*918_*935delinsCTATGTGATCAAGAAATC	ENSP00000516675.1:n.*918_*935delinsCTATGTGATCAAGAAATC
ENST00000686459.1:c.*469_*486delinsCTATGTGATCAAGAAATC	ENSP00000508909.1:n.*469_*486delinsCTATGTGATCAAGAAATC
ENST00000688158.1:c.*994_*1011delinsCTATGTGATCAAGAAATC	ENSP00000509254.1:n.*994_*1011delinsCTATGTGATCAAGAAATC
ENST00000688308.1:c.883_900delinsCTATGTGATCAAGAAATC	ENSP00000508752.1:p.Leu295=
ENST00000688922.1:c.804_821delinsCTATGTGATCAAGAAATC
ENST00000693560.1:c.1402_1419delinsCTATGTGATCAAGAAATC	ENSP00000509861.1:p.Leu468=
ENST00000371953.8:c.883_900delinsCTATGTGATCAAGAAATC MANE Select	ENSP00000361021.3:p.Leu295=
ENST00000371953.7:c.883_900delinsCTATGTGATCAAGAAATC	ENSP00000361021.3:p.Leu295=
ENST00000472832.2:c.310_327delinsCTATGTGATCAAGAAATC	ENSP00000483066.1:p.Leu104=
NM_000314.5:c.883_900delinsCTATGTGATCAAGAAATC	NP_000305.3:p.Leu295=
NM_000314.6:c.883_900delinsCTATGTGATCAAGAAATC	NP_000305.3:p.Leu295=
NM_001304717.2:c.1402_1419delinsCTATGTGATCAAGAAATC	NP_001291646.2:p.Leu468=
NM_001304718.1:c.292_309delinsCTATGTGATCAAGAAATC	NP_001291647.1:p.Leu98=
XM_006717926.2:c.838_855delinsCTATGTGATCAAGAAATC	XP_006717989.1:p.Leu280=
XM_011539981.1:c.883_900delinsCTATGTGATCAAGAAATC	XP_011538283.1:p.Leu295=
XM_011539982.1:c.787_804delinsCTATGTGATCAAGAAATC	XP_011538284.1:p.Leu263=
XR_945791.1:n.1453_1470delinsCTATGTGATCAAGAAATC
NM_000314.7:c.883_900delinsCTATGTGATCAAGAAATC	NP_000305.3:p.Leu295=
NM_001304717.5:c.1402_1419delinsCTATGTGATCAAGAAATC	NP_001291646.4:p.Leu468=
NM_001304718.2:c.292_309delinsCTATGTGATCAAGAAATC	NP_001291647.1:p.Leu98=
NM_000314.8:c.883_900delinsCTATGTGATCAAGAAATC MANE Select	NP_000305.3:p.Leu295=