Canonical Allele Identifier: CA891836757

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961068_87961070delinsTCT , CM000672.2:g.87961068_87961070delinsTCT	GRCh38
NC_000010.10:g.89720825_89720827delinsTCT , CM000672.1:g.89720825_89720827delinsTCT	GRCh37
NC_000010.9:g.89710805_89710807delinsTCT	NCBI36
NG_007466.2:g.102630_102632delinsTCT , LRG_311:g.102630_102632delinsTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1069_1071delinsTCT	ENSP00000514759.2:p.Asp357Ser
ENST00000710265.1:c.976_978delinsTCT	ENSP00000518161.1:p.Asp326Ser
ENST00000472832.3:c.976_978delinsTCT	ENSP00000483066.2:p.Asp326Ser
ENST00000688158.2:n.1711_1713delinsTCT
ENST00000688922.2:c.*806_*808delinsTCT	ENSP00000508742.2:n.*806_*808delinsTCT
ENST00000700021.1:c.931_933delinsTCT	ENSP00000514757.1:p.Asp311Ser
ENST00000700022.1:c.*315_*317delinsTCT	ENSP00000514758.1:n.*315_*317delinsTCT
ENST00000700023.1:n.2134_2136delinsTCT
ENST00000700024.1:n.2368_2370delinsTCT
ENST00000700025.1:n.1745_1747delinsTCT
ENST00000700026.1:n.613_615delinsTCT
ENST00000706954.1:c.976_978delinsTCT	ENSP00000516674.1:p.Asp326Ser
ENST00000706955.1:c.*1011_*1013delinsTCT	ENSP00000516675.1:n.*1011_*1013delinsTCT
ENST00000686459.1:c.*562_*564delinsTCT	ENSP00000508909.1:n.*562_*564delinsTCT
ENST00000688158.1:c.*1087_*1089delinsTCT	ENSP00000509254.1:n.*1087_*1089delinsTCT
ENST00000688308.1:c.976_978delinsTCT	ENSP00000508752.1:p.Asp326Ser
ENST00000688922.1:c.897_899delinsTCT
ENST00000693560.1:c.1495_1497delinsTCT	ENSP00000509861.1:p.Asp499Ser
ENST00000371953.8:c.976_978delinsTCT MANE Select	ENSP00000361021.3:p.Asp326Ser
ENST00000371953.7:c.976_978delinsTCT	ENSP00000361021.3:p.Asp326Ser
ENST00000472832.2:c.403_405delinsTCT	ENSP00000483066.1:p.Asp135Ser
NM_000314.5:c.976_978delinsTCT	NP_000305.3:p.Asp326Ser
NM_000314.6:c.976_978delinsTCT	NP_000305.3:p.Asp326Ser
NM_001304717.2:c.1495_1497delinsTCT	NP_001291646.2:p.Asp499Ser
NM_001304718.1:c.385_387delinsTCT	NP_001291647.1:p.Asp129Ser
XM_006717926.2:c.931_933delinsTCT	XP_006717989.1:p.Asp311Ser
XM_011539981.1:c.976_978delinsTCT	XP_011538283.1:p.Asp326Ser
XM_011539982.1:c.880_882delinsTCT	XP_011538284.1:p.Asp294Ser
XR_945791.1:n.1546_1548delinsTCT
NM_000314.7:c.976_978delinsTCT	NP_000305.3:p.Asp326Ser
NM_001304717.5:c.1495_1497delinsTCT	NP_001291646.4:p.Asp499Ser
NM_001304718.2:c.385_387delinsTCT	NP_001291647.1:p.Asp129Ser
NM_000314.8:c.976_978delinsTCT MANE Select	NP_000305.3:p.Asp326Ser