Canonical Allele Identifier: CA891841354

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961086_87961088delinsTGG , CM000672.2:g.87961086_87961088delinsTGG	GRCh38
NC_000010.10:g.89720843_89720845delinsTGG , CM000672.1:g.89720843_89720845delinsTGG	GRCh37
NC_000010.9:g.89710823_89710825delinsTGG	NCBI36
NG_007466.2:g.102648_102650delinsTGG , LRG_311:g.102648_102650delinsTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1087_1089delinsTGG	ENSP00000514759.2:p.Lys363Trp
ENST00000710265.1:c.994_996delinsTGG	ENSP00000518161.1:p.Lys332Trp
ENST00000472832.3:c.994_996delinsTGG	ENSP00000483066.2:p.Lys332Trp
ENST00000688158.2:n.1729_1731delinsTGG
ENST00000688922.2:c.*824_*826delinsTGG	ENSP00000508742.2:n.*824_*826delinsTGG
ENST00000700021.1:c.949_951delinsTGG	ENSP00000514757.1:p.Lys317Trp
ENST00000700022.1:c.*333_*335delinsTGG	ENSP00000514758.1:n.*333_*335delinsTGG
ENST00000700023.1:n.2152_2154delinsTGG
ENST00000700024.1:n.2386_2388delinsTGG
ENST00000700025.1:n.1763_1765delinsTGG
ENST00000700026.1:n.631_633delinsTGG
ENST00000706954.1:c.994_996delinsTGG	ENSP00000516674.1:p.Lys332Trp
ENST00000706955.1:c.*1029_*1031delinsTGG	ENSP00000516675.1:n.*1029_*1031delinsTGG
ENST00000686459.1:c.*580_*582delinsTGG	ENSP00000508909.1:n.*580_*582delinsTGG
ENST00000688158.1:c.*1105_*1107delinsTGG	ENSP00000509254.1:n.*1105_*1107delinsTGG
ENST00000688308.1:c.994_996delinsTGG	ENSP00000508752.1:p.Lys332Trp
ENST00000688922.1:c.915_917delinsTGG
ENST00000693560.1:c.1513_1515delinsTGG	ENSP00000509861.1:p.Lys505Trp
ENST00000371953.8:c.994_996delinsTGG MANE Select	ENSP00000361021.3:p.Lys332Trp
ENST00000371953.7:c.994_996delinsTGG	ENSP00000361021.3:p.Lys332Trp
ENST00000472832.2:c.421_423delinsTGG	ENSP00000483066.1:p.Lys141Trp
NM_000314.5:c.994_996delinsTGG	NP_000305.3:p.Lys332Trp
NM_000314.6:c.994_996delinsTGG	NP_000305.3:p.Lys332Trp
NM_001304717.2:c.1513_1515delinsTGG	NP_001291646.2:p.Lys505Trp
NM_001304718.1:c.403_405delinsTGG	NP_001291647.1:p.Lys135Trp
XM_006717926.2:c.949_951delinsTGG	XP_006717989.1:p.Lys317Trp
XM_011539981.1:c.994_996delinsTGG	XP_011538283.1:p.Lys332Trp
XM_011539982.1:c.898_900delinsTGG	XP_011538284.1:p.Lys300Trp
XR_945791.1:n.1564_1566delinsTGG
NM_000314.7:c.994_996delinsTGG	NP_000305.3:p.Lys332Trp
NM_001304717.5:c.1513_1515delinsTGG	NP_001291646.4:p.Lys505Trp
NM_001304718.2:c.403_405delinsTGG	NP_001291647.1:p.Lys135Trp
NM_000314.8:c.994_996delinsTGG MANE Select	NP_000305.3:p.Lys332Trp