Canonical Allele Identifier: CA2579926802

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960897_87960899delinsGGT , CM000672.2:g.87960897_87960899delinsGGT	GRCh38
NC_000010.10:g.89720654_89720656delinsGGT , CM000672.1:g.89720654_89720656delinsGGT	GRCh37
NC_000010.9:g.89710634_89710636delinsGGT	NCBI36
NG_007466.2:g.102459_102461delinsGGT , LRG_311:g.102459_102461delinsGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.898_900delinsGGT	ENSP00000514759.2:p.Lys300Gly
ENST00000710265.1:c.805_807delinsGGT	ENSP00000518161.1:p.Lys269Gly
ENST00000472832.3:c.805_807delinsGGT	ENSP00000483066.2:p.Lys269Gly
ENST00000688158.2:n.1540_1542delinsGGT
ENST00000688922.2:c.*635_*637delinsGGT	ENSP00000508742.2:n.*635_*637delinsGGT
ENST00000700021.1:c.760_762delinsGGT	ENSP00000514757.1:p.Lys254Gly
ENST00000700022.1:c.*144_*146delinsGGT	ENSP00000514758.1:n.*144_*146delinsGGT
ENST00000700023.1:n.1963_1965delinsGGT
ENST00000700024.1:n.2197_2199delinsGGT
ENST00000700025.1:n.1574_1576delinsGGT
ENST00000700026.1:n.442_444delinsGGT
ENST00000700029.1:c.732_734delinsGGT
ENST00000706954.1:c.805_807delinsGGT	ENSP00000516674.1:p.Lys269Gly
ENST00000706955.1:c.*840_*842delinsGGT	ENSP00000516675.1:n.*840_*842delinsGGT
ENST00000686459.1:c.*391_*393delinsGGT	ENSP00000508909.1:n.*391_*393delinsGGT
ENST00000688158.1:c.*916_*918delinsGGT	ENSP00000509254.1:n.*916_*918delinsGGT
ENST00000688308.1:c.805_807delinsGGT	ENSP00000508752.1:p.Lys269Gly
ENST00000688922.1:c.726_728delinsGGT
ENST00000693560.1:c.1324_1326delinsGGT	ENSP00000509861.1:p.Lys442Gly
ENST00000371953.8:c.805_807delinsGGT MANE Select	ENSP00000361021.3:p.Lys269Gly
ENST00000371953.7:c.805_807delinsGGT	ENSP00000361021.3:p.Lys269Gly
ENST00000472832.2:c.232_234delinsGGT	ENSP00000483066.1:p.Lys78Gly
NM_000314.5:c.805_807delinsGGT	NP_000305.3:p.Lys269Gly
NM_000314.6:c.805_807delinsGGT	NP_000305.3:p.Lys269Gly
NM_001304717.2:c.1324_1326delinsGGT	NP_001291646.2:p.Lys442Gly
NM_001304718.1:c.214_216delinsGGT	NP_001291647.1:p.Lys72Gly
XM_006717926.2:c.760_762delinsGGT	XP_006717989.1:p.Lys254Gly
XM_011539981.1:c.805_807delinsGGT	XP_011538283.1:p.Lys269Gly
XM_011539982.1:c.709_711delinsGGT	XP_011538284.1:p.Lys237Gly
XR_945791.1:n.1375_1377delinsGGT
NM_000314.7:c.805_807delinsGGT	NP_000305.3:p.Lys269Gly
NM_001304717.5:c.1324_1326delinsGGT	NP_001291646.4:p.Lys442Gly
NM_001304718.2:c.214_216delinsGGT	NP_001291647.1:p.Lys72Gly
NM_000314.8:c.805_807delinsGGT MANE Select	NP_000305.3:p.Lys269Gly