Canonical Allele Identifier: CA891839098

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952215_87952216delinsTT , CM000672.2:g.87952215_87952216delinsTT	GRCh38
NC_000010.10:g.89711972_89711973delinsTT , CM000672.1:g.89711972_89711973delinsTT	GRCh37
NC_000010.9:g.89701952_89701953delinsTT	NCBI36
NG_007466.2:g.93777_93778delinsTT , LRG_311:g.93777_93778delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.590_591delinsTT	ENSP00000514759.2:p.Lys197Ile
ENST00000710265.1:c.590_591delinsTT	ENSP00000518161.1:p.Lys197Ile
ENST00000472832.3:c.590_591delinsTT	ENSP00000483066.2:p.Lys197Ile
ENST00000688158.2:n.1325_1326delinsTT
ENST00000688922.2:c.*420_*421delinsTT	ENSP00000508742.2:n.*420_*421delinsTT
ENST00000700021.1:c.545_546delinsTT	ENSP00000514757.1:p.Lys182Ile
ENST00000700022.1:c.493-5638_493-5637delinsTT	ENSP00000514758.1:n.493-5638_493-5637delinsTT
ENST00000700023.1:n.1748_1749delinsTT
ENST00000700024.1:n.1982_1983delinsTT
ENST00000700025.1:n.1359_1360delinsTT
ENST00000700029.1:c.424_425delinsTT
ENST00000706954.1:c.590_591delinsTT	ENSP00000516674.1:p.Lys197Ile
ENST00000706955.1:c.*625_*626delinsTT	ENSP00000516675.1:n.*625_*626delinsTT
ENST00000686459.1:c.*176_*177delinsTT	ENSP00000508909.1:n.*176_*177delinsTT
ENST00000688158.1:c.*701_*702delinsTT	ENSP00000509254.1:n.*701_*702delinsTT
ENST00000688308.1:c.590_591delinsTT	ENSP00000508752.1:p.Lys197Ile
ENST00000688922.1:c.511_512delinsTT
ENST00000693560.1:c.1109_1110delinsTT	ENSP00000509861.1:p.Lys370Ile
ENST00000371953.8:c.590_591delinsTT MANE Select	ENSP00000361021.3:p.Lys197Ile
ENST00000371953.7:c.590_591delinsTT	ENSP00000361021.3:p.Lys197Ile
ENST00000472832.2:c.17_18delinsTT	ENSP00000483066.1:p.Lys6Ile
NM_000314.5:c.590_591delinsTT	NP_000305.3:p.Lys197Ile
NM_000314.6:c.590_591delinsTT	NP_000305.3:p.Lys197Ile
NM_001304717.2:c.1109_1110delinsTT	NP_001291646.2:p.Lys370Ile
NM_001304718.1:c.-2_-1delinsTT	NP_001291647.1:n.-2_-1delinsTT
XM_006717926.2:c.545_546delinsTT	XP_006717989.1:p.Lys182Ile
XM_011539981.1:c.590_591delinsTT	XP_011538283.1:p.Lys197Ile
XM_011539982.1:c.494_495delinsTT	XP_011538284.1:p.Lys165Ile
XR_945791.1:n.1205-5638_1205-5637delinsTT
NM_000314.7:c.590_591delinsTT	NP_000305.3:p.Lys197Ile
NM_001304717.5:c.1109_1110delinsTT	NP_001291646.4:p.Lys370Ile
NM_001304718.2:c.-2_-1delinsTT	NP_001291647.1:n.-2_-1delinsTT
NM_000314.8:c.590_591delinsTT MANE Select	NP_000305.3:p.Lys197Ile