Canonical Allele Identifier: CA891839089

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952214_87952216delinsTAT , CM000672.2:g.87952214_87952216delinsTAT	GRCh38
NC_000010.10:g.89711971_89711973delinsTAT , CM000672.1:g.89711971_89711973delinsTAT	GRCh37
NC_000010.9:g.89701951_89701953delinsTAT	NCBI36
NG_007466.2:g.93776_93778delinsTAT , LRG_311:g.93776_93778delinsTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.589_591delinsTAT	ENSP00000514759.2:p.Lys197Tyr
ENST00000710265.1:c.589_591delinsTAT	ENSP00000518161.1:p.Lys197Tyr
ENST00000472832.3:c.589_591delinsTAT	ENSP00000483066.2:p.Lys197Tyr
ENST00000688158.2:n.1324_1326delinsTAT
ENST00000688922.2:c.*419_*421delinsTAT	ENSP00000508742.2:n.*419_*421delinsTAT
ENST00000700021.1:c.544_546delinsTAT	ENSP00000514757.1:p.Lys182Tyr
ENST00000700022.1:c.493-5639_493-5637delinsTAT	ENSP00000514758.1:n.493-5639_493-5637delinsTAT
ENST00000700023.1:n.1747_1749delinsTAT
ENST00000700024.1:n.1981_1983delinsTAT
ENST00000700025.1:n.1358_1360delinsTAT
ENST00000700029.1:c.423_425delinsTAT
ENST00000706954.1:c.589_591delinsTAT	ENSP00000516674.1:p.Lys197Tyr
ENST00000706955.1:c.*624_*626delinsTAT	ENSP00000516675.1:n.*624_*626delinsTAT
ENST00000686459.1:c.*175_*177delinsTAT	ENSP00000508909.1:n.*175_*177delinsTAT
ENST00000688158.1:c.*700_*702delinsTAT	ENSP00000509254.1:n.*700_*702delinsTAT
ENST00000688308.1:c.589_591delinsTAT	ENSP00000508752.1:p.Lys197Tyr
ENST00000688922.1:c.510_512delinsTAT
ENST00000693560.1:c.1108_1110delinsTAT	ENSP00000509861.1:p.Lys370Tyr
ENST00000371953.8:c.589_591delinsTAT MANE Select	ENSP00000361021.3:p.Lys197Tyr
ENST00000371953.7:c.589_591delinsTAT	ENSP00000361021.3:p.Lys197Tyr
ENST00000472832.2:c.16_18delinsTAT	ENSP00000483066.1:p.Lys6Tyr
NM_000314.5:c.589_591delinsTAT	NP_000305.3:p.Lys197Tyr
NM_000314.6:c.589_591delinsTAT	NP_000305.3:p.Lys197Tyr
NM_001304717.2:c.1108_1110delinsTAT	NP_001291646.2:p.Lys370Tyr
NM_001304718.1:c.-3_-1delinsTAT	NP_001291647.1:n.-3_-1delinsTAT
XM_006717926.2:c.544_546delinsTAT	XP_006717989.1:p.Lys182Tyr
XM_011539981.1:c.589_591delinsTAT	XP_011538283.1:p.Lys197Tyr
XM_011539982.1:c.493_495delinsTAT	XP_011538284.1:p.Lys165Tyr
XR_945791.1:n.1205-5639_1205-5637delinsTAT
NM_000314.7:c.589_591delinsTAT	NP_000305.3:p.Lys197Tyr
NM_001304717.5:c.1108_1110delinsTAT	NP_001291646.4:p.Lys370Tyr
NM_001304718.2:c.-3_-1delinsTAT	NP_001291647.1:n.-3_-1delinsTAT
NM_000314.8:c.589_591delinsTAT MANE Select	NP_000305.3:p.Lys197Tyr