Canonical Allele Identifier: CA891839173

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952232_87952234delinsGAA , CM000672.2:g.87952232_87952234delinsGAA	GRCh38
NC_000010.10:g.89711989_89711991delinsGAA , CM000672.1:g.89711989_89711991delinsGAA	GRCh37
NC_000010.9:g.89701969_89701971delinsGAA	NCBI36
NG_007466.2:g.93794_93796delinsGAA , LRG_311:g.93794_93796delinsGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.607_609delinsGAA	ENSP00000514759.2:p.Ile203Glu
ENST00000710265.1:c.607_609delinsGAA	ENSP00000518161.1:p.Ile203Glu
ENST00000472832.3:c.607_609delinsGAA	ENSP00000483066.2:p.Ile203Glu
ENST00000688158.2:n.1342_1344delinsGAA
ENST00000688922.2:c.*437_*439delinsGAA	ENSP00000508742.2:n.*437_*439delinsGAA
ENST00000700021.1:c.562_564delinsGAA	ENSP00000514757.1:p.Ile188Glu
ENST00000700022.1:c.493-5621_493-5619delinsGAA	ENSP00000514758.1:n.493-5621_493-5619delinsGAA
ENST00000700023.1:n.1765_1767delinsGAA
ENST00000700024.1:n.1999_2001delinsGAA
ENST00000700025.1:n.1376_1378delinsGAA
ENST00000700029.1:c.441_443delinsGAA
ENST00000706954.1:c.607_609delinsGAA	ENSP00000516674.1:p.Ile203Glu
ENST00000706955.1:c.*642_*644delinsGAA	ENSP00000516675.1:n.*642_*644delinsGAA
ENST00000686459.1:c.*193_*195delinsGAA	ENSP00000508909.1:n.*193_*195delinsGAA
ENST00000688158.1:c.*718_*720delinsGAA	ENSP00000509254.1:n.*718_*720delinsGAA
ENST00000688308.1:c.607_609delinsGAA	ENSP00000508752.1:p.Ile203Glu
ENST00000688922.1:c.528_530delinsGAA
ENST00000693560.1:c.1126_1128delinsGAA	ENSP00000509861.1:p.Ile376Glu
ENST00000371953.8:c.607_609delinsGAA MANE Select	ENSP00000361021.3:p.Ile203Glu
ENST00000371953.7:c.607_609delinsGAA	ENSP00000361021.3:p.Ile203Glu
ENST00000472832.2:c.34_36delinsGAA	ENSP00000483066.1:p.Ile12Glu
NM_000314.5:c.607_609delinsGAA	NP_000305.3:p.Ile203Glu
NM_000314.6:c.607_609delinsGAA	NP_000305.3:p.Ile203Glu
NM_001304717.2:c.1126_1128delinsGAA	NP_001291646.2:p.Ile376Glu
NM_001304718.1:c.16_18delinsGAA	NP_001291647.1:p.Ile6Glu
XM_006717926.2:c.562_564delinsGAA	XP_006717989.1:p.Ile188Glu
XM_011539981.1:c.607_609delinsGAA	XP_011538283.1:p.Ile203Glu
XM_011539982.1:c.511_513delinsGAA	XP_011538284.1:p.Ile171Glu
XR_945791.1:n.1205-5621_1205-5619delinsGAA
NM_000314.7:c.607_609delinsGAA	NP_000305.3:p.Ile203Glu
NM_001304717.5:c.1126_1128delinsGAA	NP_001291646.4:p.Ile376Glu
NM_001304718.2:c.16_18delinsGAA	NP_001291647.1:p.Ile6Glu
NM_000314.8:c.607_609delinsGAA MANE Select	NP_000305.3:p.Ile203Glu