Canonical Allele Identifier: CA891840514

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87925550_87925551delinsGG , CM000672.2:g.87925550_87925551delinsGG	GRCh38
NC_000010.10:g.89685307_89685308delinsGG , CM000672.1:g.89685307_89685308delinsGG	GRCh37
NC_000010.9:g.89675287_89675288delinsGG	NCBI36
NG_007466.2:g.67112_67113delinsGG , LRG_311:g.67112_67113delinsGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.202_203delinsGG	ENSP00000514759.2:p.Tyr68Gly
ENST00000710265.1:c.202_203delinsGG	ENSP00000518161.1:p.Tyr68Gly
ENST00000472832.3:c.202_203delinsGG	ENSP00000483066.2:p.Tyr68Gly
ENST00000688158.2:n.937_938delinsGG
ENST00000688922.2:c.202_203delinsGG	ENSP00000508742.2:p.Tyr68Gly
ENST00000700021.1:c.165-5496_165-5495delinsGG	ENSP00000514757.1:n.165-5496_165-5495delinsGG
ENST00000700022.1:c.202_203delinsGG	ENSP00000514758.1:p.Tyr68Gly
ENST00000700029.1:c.36_37delinsGG
ENST00000706954.1:c.202_203delinsGG	ENSP00000516674.1:p.Tyr68Gly
ENST00000706955.1:c.*237_*238delinsGG	ENSP00000516675.1:n.*237_*238delinsGG
ENST00000686459.1:c.202_203delinsGG	ENSP00000508909.1:p.Tyr68Gly
ENST00000688158.1:c.*313_*314delinsGG	ENSP00000509254.1:n.*313_*314delinsGG
ENST00000688308.1:c.202_203delinsGG	ENSP00000508752.1:p.Tyr68Gly
ENST00000688922.1:c.71_72delinsGG
ENST00000693560.1:c.721_722delinsGG	ENSP00000509861.1:p.Tyr241Gly
ENST00000371953.8:c.202_203delinsGG MANE Select	ENSP00000361021.3:p.Tyr68Gly
ENST00000371953.7:c.202_203delinsGG	ENSP00000361021.3:p.Tyr68Gly
ENST00000498703.1:n.28_29delinsGG
ENST00000610634.1:c.100_101delinsGG	ENSP00000477517.1:p.Tyr34Gly
NM_000314.5:c.202_203delinsGG	NP_000305.3:p.Tyr68Gly
NM_000314.6:c.202_203delinsGG	NP_000305.3:p.Tyr68Gly
NM_001304717.2:c.721_722delinsGG	NP_001291646.2:p.Tyr241Gly
NM_001304718.1:c.-541-5496_-541-5495delinsGG	NP_001291647.1:n.-541-5496_-541-5495delinsGG
XM_006717926.2:c.165-5496_165-5495delinsGG	XP_006717989.1:n.165-5496_165-5495delinsGG
XM_011539981.1:c.202_203delinsGG	XP_011538283.1:p.Tyr68Gly
XM_011539982.1:c.106_107delinsGG	XP_011538284.1:p.Tyr36Gly
XR_945789.1:n.914_915delinsGG
XR_945790.1:n.914_915delinsGG
XR_945791.1:n.914_915delinsGG
NM_000314.7:c.202_203delinsGG	NP_000305.3:p.Tyr68Gly
NM_001304717.5:c.721_722delinsGG	NP_001291646.4:p.Tyr241Gly
NM_001304718.2:c.-541-5496_-541-5495delinsGG	NP_001291647.1:n.-541-5496_-541-5495delinsGG
NM_000314.8:c.202_203delinsGG MANE Select	NP_000305.3:p.Tyr68Gly