Canonical Allele Identifier: CA891839612

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957915_87957917delinsGGT , CM000672.2:g.87957915_87957917delinsGGT	GRCh38
NC_000010.10:g.89717672_89717674delinsGGT , CM000672.1:g.89717672_89717674delinsGGT	GRCh37
NC_000010.9:g.89707652_89707654delinsGGT	NCBI36
NG_007466.2:g.99477_99479delinsGGT , LRG_311:g.99477_99479delinsGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.697_699delinsGGT	ENSP00000514759.2:p.Arg233Gly
ENST00000710265.1:c.697_699delinsGGT	ENSP00000518161.1:p.Arg233Gly
ENST00000472832.3:c.697_699delinsGGT	ENSP00000483066.2:p.Arg233Gly
ENST00000688158.2:n.1432_1434delinsGGT
ENST00000688922.2:c.*527_*529delinsGGT	ENSP00000508742.2:n.*527_*529delinsGGT
ENST00000700021.1:c.652_654delinsGGT	ENSP00000514757.1:p.Arg218Gly
ENST00000700022.1:c.*36_*38delinsGGT	ENSP00000514758.1:n.*36_*38delinsGGT
ENST00000700023.1:n.1855_1857delinsGGT
ENST00000700024.1:n.2089_2091delinsGGT
ENST00000700025.1:n.1466_1468delinsGGT
ENST00000700026.1:n.334_336delinsGGT
ENST00000700029.1:c.531_533delinsGGT
ENST00000706954.1:c.697_699delinsGGT	ENSP00000516674.1:p.Arg233Gly
ENST00000706955.1:c.*732_*734delinsGGT	ENSP00000516675.1:n.*732_*734delinsGGT
ENST00000686459.1:c.*283_*285delinsGGT	ENSP00000508909.1:n.*283_*285delinsGGT
ENST00000688158.1:c.*808_*810delinsGGT	ENSP00000509254.1:n.*808_*810delinsGGT
ENST00000688308.1:c.697_699delinsGGT	ENSP00000508752.1:p.Arg233Gly
ENST00000688922.1:c.618_620delinsGGT
ENST00000693560.1:c.1216_1218delinsGGT	ENSP00000509861.1:p.Arg406Gly
ENST00000371953.8:c.697_699delinsGGT MANE Select	ENSP00000361021.3:p.Arg233Gly
ENST00000371953.7:c.697_699delinsGGT	ENSP00000361021.3:p.Arg233Gly
ENST00000472832.2:c.124_126delinsGGT	ENSP00000483066.1:p.Arg42Gly
NM_000314.5:c.697_699delinsGGT	NP_000305.3:p.Arg233Gly
NM_000314.6:c.697_699delinsGGT	NP_000305.3:p.Arg233Gly
NM_001304717.2:c.1216_1218delinsGGT	NP_001291646.2:p.Arg406Gly
NM_001304718.1:c.106_108delinsGGT	NP_001291647.1:p.Arg36Gly
XM_006717926.2:c.652_654delinsGGT	XP_006717989.1:p.Arg218Gly
XM_011539981.1:c.697_699delinsGGT	XP_011538283.1:p.Arg233Gly
XM_011539982.1:c.601_603delinsGGT	XP_011538284.1:p.Arg201Gly
XR_945791.1:n.1267_1269delinsGGT
NM_000314.7:c.697_699delinsGGT	NP_000305.3:p.Arg233Gly
NM_001304717.5:c.1216_1218delinsGGT	NP_001291646.4:p.Arg406Gly
NM_001304718.2:c.106_108delinsGGT	NP_001291647.1:p.Arg36Gly
NM_000314.8:c.697_699delinsGGT MANE Select	NP_000305.3:p.Arg233Gly