Canonical Allele Identifier: CA891836758

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961068_87961070delinsTGG , CM000672.2:g.87961068_87961070delinsTGG	GRCh38
NC_000010.10:g.89720825_89720827delinsTGG , CM000672.1:g.89720825_89720827delinsTGG	GRCh37
NC_000010.9:g.89710805_89710807delinsTGG	NCBI36
NG_007466.2:g.102630_102632delinsTGG , LRG_311:g.102630_102632delinsTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1069_1071delinsTGG	ENSP00000514759.2:p.Asp357Trp
ENST00000710265.1:c.976_978delinsTGG	ENSP00000518161.1:p.Asp326Trp
ENST00000472832.3:c.976_978delinsTGG	ENSP00000483066.2:p.Asp326Trp
ENST00000688158.2:n.1711_1713delinsTGG
ENST00000688922.2:c.*806_*808delinsTGG	ENSP00000508742.2:n.*806_*808delinsTGG
ENST00000700021.1:c.931_933delinsTGG	ENSP00000514757.1:p.Asp311Trp
ENST00000700022.1:c.*315_*317delinsTGG	ENSP00000514758.1:n.*315_*317delinsTGG
ENST00000700023.1:n.2134_2136delinsTGG
ENST00000700024.1:n.2368_2370delinsTGG
ENST00000700025.1:n.1745_1747delinsTGG
ENST00000700026.1:n.613_615delinsTGG
ENST00000706954.1:c.976_978delinsTGG	ENSP00000516674.1:p.Asp326Trp
ENST00000706955.1:c.*1011_*1013delinsTGG	ENSP00000516675.1:n.*1011_*1013delinsTGG
ENST00000686459.1:c.*562_*564delinsTGG	ENSP00000508909.1:n.*562_*564delinsTGG
ENST00000688158.1:c.*1087_*1089delinsTGG	ENSP00000509254.1:n.*1087_*1089delinsTGG
ENST00000688308.1:c.976_978delinsTGG	ENSP00000508752.1:p.Asp326Trp
ENST00000688922.1:c.897_899delinsTGG
ENST00000693560.1:c.1495_1497delinsTGG	ENSP00000509861.1:p.Asp499Trp
ENST00000371953.8:c.976_978delinsTGG MANE Select	ENSP00000361021.3:p.Asp326Trp
ENST00000371953.7:c.976_978delinsTGG	ENSP00000361021.3:p.Asp326Trp
ENST00000472832.2:c.403_405delinsTGG	ENSP00000483066.1:p.Asp135Trp
NM_000314.5:c.976_978delinsTGG	NP_000305.3:p.Asp326Trp
NM_000314.6:c.976_978delinsTGG	NP_000305.3:p.Asp326Trp
NM_001304717.2:c.1495_1497delinsTGG	NP_001291646.2:p.Asp499Trp
NM_001304718.1:c.385_387delinsTGG	NP_001291647.1:p.Asp129Trp
XM_006717926.2:c.931_933delinsTGG	XP_006717989.1:p.Asp311Trp
XM_011539981.1:c.976_978delinsTGG	XP_011538283.1:p.Asp326Trp
XM_011539982.1:c.880_882delinsTGG	XP_011538284.1:p.Asp294Trp
XR_945791.1:n.1546_1548delinsTGG
NM_000314.7:c.976_978delinsTGG	NP_000305.3:p.Asp326Trp
NM_001304717.5:c.1495_1497delinsTGG	NP_001291646.4:p.Asp499Trp
NM_001304718.2:c.385_387delinsTGG	NP_001291647.1:p.Asp129Trp
NM_000314.8:c.976_978delinsTGG MANE Select	NP_000305.3:p.Asp326Trp