Canonical Allele Identifier: CA891835249

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87925550_87925552delinsGCT , CM000672.2:g.87925550_87925552delinsGCT	GRCh38
NC_000010.10:g.89685307_89685309delinsGCT , CM000672.1:g.89685307_89685309delinsGCT	GRCh37
NC_000010.9:g.89675287_89675289delinsGCT	NCBI36
NG_007466.2:g.67112_67114delinsGCT , LRG_311:g.67112_67114delinsGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.202_204delinsGCT	ENSP00000514759.2:p.Tyr68Ala
ENST00000710265.1:c.202_204delinsGCT	ENSP00000518161.1:p.Tyr68Ala
ENST00000472832.3:c.202_204delinsGCT	ENSP00000483066.2:p.Tyr68Ala
ENST00000688158.2:n.937_939delinsGCT
ENST00000688922.2:c.202_204delinsGCT	ENSP00000508742.2:p.Tyr68Ala
ENST00000700021.1:c.165-5496_165-5494delinsGCT	ENSP00000514757.1:n.165-5496_165-5494delinsGCT
ENST00000700022.1:c.202_204delinsGCT	ENSP00000514758.1:p.Tyr68Ala
ENST00000700029.1:c.36_38delinsGCT
ENST00000706954.1:c.202_204delinsGCT	ENSP00000516674.1:p.Tyr68Ala
ENST00000706955.1:c.*237_*239delinsGCT	ENSP00000516675.1:n.*237_*239delinsGCT
ENST00000686459.1:c.202_204delinsGCT	ENSP00000508909.1:p.Tyr68Ala
ENST00000688158.1:c.*313_*315delinsGCT	ENSP00000509254.1:n.*313_*315delinsGCT
ENST00000688308.1:c.202_204delinsGCT	ENSP00000508752.1:p.Tyr68Ala
ENST00000688922.1:c.71_73delinsGCT
ENST00000693560.1:c.721_723delinsGCT	ENSP00000509861.1:p.Tyr241Ala
ENST00000371953.8:c.202_204delinsGCT MANE Select	ENSP00000361021.3:p.Tyr68Ala
ENST00000371953.7:c.202_204delinsGCT	ENSP00000361021.3:p.Tyr68Ala
ENST00000498703.1:n.28_30delinsGCT
ENST00000610634.1:c.100_102delinsGCT	ENSP00000477517.1:p.Tyr34Ala
NM_000314.5:c.202_204delinsGCT	NP_000305.3:p.Tyr68Ala
NM_000314.6:c.202_204delinsGCT	NP_000305.3:p.Tyr68Ala
NM_001304717.2:c.721_723delinsGCT	NP_001291646.2:p.Tyr241Ala
NM_001304718.1:c.-541-5496_-541-5494delinsGCT	NP_001291647.1:n.-541-5496_-541-5494delinsGCT
XM_006717926.2:c.165-5496_165-5494delinsGCT	XP_006717989.1:n.165-5496_165-5494delinsGCT
XM_011539981.1:c.202_204delinsGCT	XP_011538283.1:p.Tyr68Ala
XM_011539982.1:c.106_108delinsGCT	XP_011538284.1:p.Tyr36Ala
XR_945789.1:n.914_916delinsGCT
XR_945790.1:n.914_916delinsGCT
XR_945791.1:n.914_916delinsGCT
NM_000314.7:c.202_204delinsGCT	NP_000305.3:p.Tyr68Ala
NM_001304717.5:c.721_723delinsGCT	NP_001291646.4:p.Tyr241Ala
NM_001304718.2:c.-541-5496_-541-5494delinsGCT	NP_001291647.1:n.-541-5496_-541-5494delinsGCT
NM_000314.8:c.202_204delinsGCT MANE Select	NP_000305.3:p.Tyr68Ala