Canonical Allele Identifier: CA2579926660

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961087_87961088delinsCT , CM000672.2:g.87961087_87961088delinsCT	GRCh38
NC_000010.10:g.89720844_89720845delinsCT , CM000672.1:g.89720844_89720845delinsCT	GRCh37
NC_000010.9:g.89710824_89710825delinsCT	NCBI36
NG_007466.2:g.102649_102650delinsCT , LRG_311:g.102649_102650delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1088_1089delinsCT	ENSP00000514759.2:p.Lys363Thr
ENST00000710265.1:c.995_996delinsCT	ENSP00000518161.1:p.Lys332Thr
ENST00000472832.3:c.995_996delinsCT	ENSP00000483066.2:p.Lys332Thr
ENST00000688158.2:n.1730_1731delinsCT
ENST00000688922.2:c.*825_*826delinsCT	ENSP00000508742.2:n.*825_*826delinsCT
ENST00000700021.1:c.950_951delinsCT	ENSP00000514757.1:p.Lys317Thr
ENST00000700022.1:c.*334_*335delinsCT	ENSP00000514758.1:n.*334_*335delinsCT
ENST00000700023.1:n.2153_2154delinsCT
ENST00000700024.1:n.2387_2388delinsCT
ENST00000700025.1:n.1764_1765delinsCT
ENST00000700026.1:n.632_633delinsCT
ENST00000706954.1:c.995_996delinsCT	ENSP00000516674.1:p.Lys332Thr
ENST00000706955.1:c.*1030_*1031delinsCT	ENSP00000516675.1:n.*1030_*1031delinsCT
ENST00000686459.1:c.*581_*582delinsCT	ENSP00000508909.1:n.*581_*582delinsCT
ENST00000688158.1:c.*1106_*1107delinsCT	ENSP00000509254.1:n.*1106_*1107delinsCT
ENST00000688308.1:c.995_996delinsCT	ENSP00000508752.1:p.Lys332Thr
ENST00000688922.1:c.916_917delinsCT
ENST00000693560.1:c.1514_1515delinsCT	ENSP00000509861.1:p.Lys505Thr
ENST00000371953.8:c.995_996delinsCT MANE Select	ENSP00000361021.3:p.Lys332Thr
ENST00000371953.7:c.995_996delinsCT	ENSP00000361021.3:p.Lys332Thr
ENST00000472832.2:c.422_423delinsCT	ENSP00000483066.1:p.Lys141Thr
NM_000314.5:c.995_996delinsCT	NP_000305.3:p.Lys332Thr
NM_000314.6:c.995_996delinsCT	NP_000305.3:p.Lys332Thr
NM_001304717.2:c.1514_1515delinsCT	NP_001291646.2:p.Lys505Thr
NM_001304718.1:c.404_405delinsCT	NP_001291647.1:p.Lys135Thr
XM_006717926.2:c.950_951delinsCT	XP_006717989.1:p.Lys317Thr
XM_011539981.1:c.995_996delinsCT	XP_011538283.1:p.Lys332Thr
XM_011539982.1:c.899_900delinsCT	XP_011538284.1:p.Lys300Thr
XR_945791.1:n.1565_1566delinsCT
NM_000314.7:c.995_996delinsCT	NP_000305.3:p.Lys332Thr
NM_001304717.5:c.1514_1515delinsCT	NP_001291646.4:p.Lys505Thr
NM_001304718.2:c.404_405delinsCT	NP_001291647.1:p.Lys135Thr
NM_000314.8:c.995_996delinsCT MANE Select	NP_000305.3:p.Lys332Thr