Canonical Allele Identifier: CA2579926622

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961095_87961097delinsGAT , CM000672.2:g.87961095_87961097delinsGAT	GRCh38
NC_000010.10:g.89720852_89720854delinsGAT , CM000672.1:g.89720852_89720854delinsGAT	GRCh37
NC_000010.9:g.89710832_89710834delinsGAT	NCBI36
NG_007466.2:g.102657_102659delinsGAT , LRG_311:g.102657_102659delinsGAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.1096_1098delinsGAT	ENSP00000514759.2:p.Arg366Asp
ENST00000710265.1:c.1003_1005delinsGAT	ENSP00000518161.1:p.Arg335Asp
ENST00000472832.3:c.1003_1005delinsGAT	ENSP00000483066.2:p.Arg335Asp
ENST00000688158.2:n.1738_1740delinsGAT
ENST00000688922.2:c.*833_*835delinsGAT	ENSP00000508742.2:n.*833_*835delinsGAT
ENST00000700021.1:c.958_960delinsGAT	ENSP00000514757.1:p.Arg320Asp
ENST00000700022.1:c.*342_*344delinsGAT	ENSP00000514758.1:n.*342_*344delinsGAT
ENST00000700023.1:n.2161_2163delinsGAT
ENST00000700024.1:n.2395_2397delinsGAT
ENST00000700025.1:n.1772_1774delinsGAT
ENST00000700026.1:n.640_642delinsGAT
ENST00000706954.1:c.1003_1005delinsGAT	ENSP00000516674.1:p.Arg335Asp
ENST00000706955.1:c.*1038_*1040delinsGAT	ENSP00000516675.1:n.*1038_*1040delinsGAT
ENST00000686459.1:c.*589_*591delinsGAT	ENSP00000508909.1:n.*589_*591delinsGAT
ENST00000688158.1:c.*1114_*1116delinsGAT	ENSP00000509254.1:n.*1114_*1116delinsGAT
ENST00000688308.1:c.1003_1005delinsGAT	ENSP00000508752.1:p.Arg335Asp
ENST00000688922.1:c.924_926delinsGAT
ENST00000693560.1:c.1522_1524delinsGAT	ENSP00000509861.1:p.Arg508Asp
ENST00000371953.8:c.1003_1005delinsGAT MANE Select	ENSP00000361021.3:p.Arg335Asp
ENST00000371953.7:c.1003_1005delinsGAT	ENSP00000361021.3:p.Arg335Asp
ENST00000472832.2:c.430_432delinsGAT	ENSP00000483066.1:p.Arg144Asp
NM_000314.5:c.1003_1005delinsGAT	NP_000305.3:p.Arg335Asp
NM_000314.6:c.1003_1005delinsGAT	NP_000305.3:p.Arg335Asp
NM_001304717.2:c.1522_1524delinsGAT	NP_001291646.2:p.Arg508Asp
NM_001304718.1:c.412_414delinsGAT	NP_001291647.1:p.Arg138Asp
XM_006717926.2:c.958_960delinsGAT	XP_006717989.1:p.Arg320Asp
XM_011539981.1:c.1003_1005delinsGAT	XP_011538283.1:p.Arg335Asp
XM_011539982.1:c.907_909delinsGAT	XP_011538284.1:p.Arg303Asp
XR_945791.1:n.1573_1575delinsGAT
NM_000314.7:c.1003_1005delinsGAT	NP_000305.3:p.Arg335Asp
NM_001304717.5:c.1522_1524delinsGAT	NP_001291646.4:p.Arg508Asp
NM_001304718.2:c.412_414delinsGAT	NP_001291647.1:p.Arg138Asp
NM_000314.8:c.1003_1005delinsGAT MANE Select	NP_000305.3:p.Arg335Asp