Canonical Allele Identifier: CA891836909

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961086_87961088delinsGTT , CM000672.2:g.87961086_87961088delinsGTT	GRCh38
NC_000010.10:g.89720843_89720845delinsGTT , CM000672.1:g.89720843_89720845delinsGTT	GRCh37
NC_000010.9:g.89710823_89710825delinsGTT	NCBI36
NG_007466.2:g.102648_102650delinsGTT , LRG_311:g.102648_102650delinsGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1087_1089delinsGTT	ENSP00000514759.2:p.Lys363Val
ENST00000710265.1:c.994_996delinsGTT	ENSP00000518161.1:p.Lys332Val
ENST00000472832.3:c.994_996delinsGTT	ENSP00000483066.2:p.Lys332Val
ENST00000688158.2:n.1729_1731delinsGTT
ENST00000688922.2:c.*824_*826delinsGTT	ENSP00000508742.2:n.*824_*826delinsGTT
ENST00000700021.1:c.949_951delinsGTT	ENSP00000514757.1:p.Lys317Val
ENST00000700022.1:c.*333_*335delinsGTT	ENSP00000514758.1:n.*333_*335delinsGTT
ENST00000700023.1:n.2152_2154delinsGTT
ENST00000700024.1:n.2386_2388delinsGTT
ENST00000700025.1:n.1763_1765delinsGTT
ENST00000700026.1:n.631_633delinsGTT
ENST00000706954.1:c.994_996delinsGTT	ENSP00000516674.1:p.Lys332Val
ENST00000706955.1:c.*1029_*1031delinsGTT	ENSP00000516675.1:n.*1029_*1031delinsGTT
ENST00000686459.1:c.*580_*582delinsGTT	ENSP00000508909.1:n.*580_*582delinsGTT
ENST00000688158.1:c.*1105_*1107delinsGTT	ENSP00000509254.1:n.*1105_*1107delinsGTT
ENST00000688308.1:c.994_996delinsGTT	ENSP00000508752.1:p.Lys332Val
ENST00000688922.1:c.915_917delinsGTT
ENST00000693560.1:c.1513_1515delinsGTT	ENSP00000509861.1:p.Lys505Val
ENST00000371953.8:c.994_996delinsGTT MANE Select	ENSP00000361021.3:p.Lys332Val
ENST00000371953.7:c.994_996delinsGTT	ENSP00000361021.3:p.Lys332Val
ENST00000472832.2:c.421_423delinsGTT	ENSP00000483066.1:p.Lys141Val
NM_000314.5:c.994_996delinsGTT	NP_000305.3:p.Lys332Val
NM_000314.6:c.994_996delinsGTT	NP_000305.3:p.Lys332Val
NM_001304717.2:c.1513_1515delinsGTT	NP_001291646.2:p.Lys505Val
NM_001304718.1:c.403_405delinsGTT	NP_001291647.1:p.Lys135Val
XM_006717926.2:c.949_951delinsGTT	XP_006717989.1:p.Lys317Val
XM_011539981.1:c.994_996delinsGTT	XP_011538283.1:p.Lys332Val
XM_011539982.1:c.898_900delinsGTT	XP_011538284.1:p.Lys300Val
XR_945791.1:n.1564_1566delinsGTT
NM_000314.7:c.994_996delinsGTT	NP_000305.3:p.Lys332Val
NM_001304717.5:c.1513_1515delinsGTT	NP_001291646.4:p.Lys505Val
NM_001304718.2:c.403_405delinsGTT	NP_001291647.1:p.Lys135Val
NM_000314.8:c.994_996delinsGTT MANE Select	NP_000305.3:p.Lys332Val