Canonical Allele Identifier: CA891840670

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87864542_87864544delinsTTG , CM000672.2:g.87864542_87864544delinsTTG	GRCh38
NC_000010.10:g.89624299_89624301delinsTTG , CM000672.1:g.89624299_89624301delinsTTG	GRCh37
NC_000010.9:g.89614279_89614281delinsTTG	NCBI36
NG_007466.2:g.6104_6106delinsTTG , LRG_311:g.6104_6106delinsTTG
NG_033079.1:g.3894_3896delinsCAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.73_75delinsTTG	ENSP00000514759.2:p.Leu25=
ENST00000710265.1:c.73_75delinsTTG	ENSP00000518161.1:p.Leu25=
ENST00000472832.3:c.73_75delinsTTG	ENSP00000483066.2:p.Leu25=
ENST00000688922.2:c.73_75delinsTTG	ENSP00000508742.2:p.Leu25=
ENST00000700021.1:c.73_75delinsTTG	ENSP00000514757.1:p.Leu25=
ENST00000700022.1:c.73_75delinsTTG	ENSP00000514758.1:p.Leu25=
ENST00000706954.1:c.73_75delinsTTG	ENSP00000516674.1:p.Leu25=
ENST00000706955.1:c.73_75delinsTTG	ENSP00000516675.1:p.Leu25=
ENST00000686459.1:c.73_75delinsTTG	ENSP00000508909.1:p.Leu25=
ENST00000688158.1:c.73_75delinsTTG	ENSP00000509254.1:p.Leu25=
ENST00000688308.1:c.73_75delinsTTG	ENSP00000508752.1:p.Leu25=
ENST00000693560.1:c.592_594delinsTTG	ENSP00000509861.1:p.Leu198=
ENST00000371953.8:c.73_75delinsTTG MANE Select	ENSP00000361021.3:p.Leu25=
ENST00000371953.7:c.73_75delinsTTG	ENSP00000361021.3:p.Leu25=
ENST00000462694.1:n.75_77delinsTTG
ENST00000487939.1:n.94_96delinsTTG
ENST00000610634.1:c.-30_-28delinsTTG	ENSP00000477517.1:n.-30_-28delinsTTG
ENST00000618586.1:n.42_44delinsTTG
NM_000314.5:c.73_75delinsTTG	NP_000305.3:p.Leu25=
NM_000314.6:c.73_75delinsTTG	NP_000305.3:p.Leu25=
NM_001304717.2:c.592_594delinsTTG	NP_001291646.2:p.Leu198=
NM_001304718.1:c.-633_-631delinsTTG	NP_001291647.1:n.-633_-631delinsTTG
XM_006717926.2:c.73_75delinsTTG	XP_006717989.1:p.Leu25=
XM_011539981.1:c.73_75delinsTTG	XP_011538283.1:p.Leu25=
XR_945789.1:n.785_787delinsTTG
XR_945790.1:n.785_787delinsTTG
XR_945791.1:n.785_787delinsTTG
NM_000314.7:c.73_75delinsTTG	NP_000305.3:p.Leu25=
NM_001304717.5:c.592_594delinsTTG	NP_001291646.4:p.Leu198=
NM_001304718.2:c.-633_-631delinsTTG	NP_001291647.1:n.-633_-631delinsTTG
NM_000314.8:c.73_75delinsTTG MANE Select	NP_000305.3:p.Leu25=