Canonical Allele Identifier: CA891837400

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87933126_87933128delinsGAT , CM000672.2:g.87933126_87933128delinsGAT	GRCh38
NC_000010.10:g.89692883_89692885delinsGAT , CM000672.1:g.89692883_89692885delinsGAT	GRCh37
NC_000010.9:g.89682863_89682865delinsGAT	NCBI36
NG_007466.2:g.74688_74690delinsGAT , LRG_311:g.74688_74690delinsGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.367_369delinsGAT	ENSP00000514759.2:p.His123Asp
ENST00000710265.1:c.367_369delinsGAT	ENSP00000518161.1:p.His123Asp
ENST00000472832.3:c.367_369delinsGAT	ENSP00000483066.2:p.His123Asp
ENST00000688158.2:n.1102_1104delinsGAT
ENST00000688922.2:c.*197_*199delinsGAT	ENSP00000508742.2:n.*197_*199delinsGAT
ENST00000700021.1:c.322_324delinsGAT	ENSP00000514757.1:p.His108Asp
ENST00000700022.1:c.367_369delinsGAT	ENSP00000514758.1:p.His123Asp
ENST00000700029.1:c.201_203delinsGAT
ENST00000706954.1:c.367_369delinsGAT	ENSP00000516674.1:p.His123Asp
ENST00000706955.1:c.*402_*404delinsGAT	ENSP00000516675.1:n.*402_*404delinsGAT
ENST00000686459.1:c.367_369delinsGAT	ENSP00000508909.1:p.His123Asp
ENST00000688158.1:c.*478_*480delinsGAT	ENSP00000509254.1:n.*478_*480delinsGAT
ENST00000688308.1:c.367_369delinsGAT	ENSP00000508752.1:p.His123Asp
ENST00000688922.1:c.288_290delinsGAT
ENST00000693560.1:c.886_888delinsGAT	ENSP00000509861.1:p.His296Asp
ENST00000371953.8:c.367_369delinsGAT MANE Select	ENSP00000361021.3:p.His123Asp
ENST00000371953.7:c.367_369delinsGAT	ENSP00000361021.3:p.His123Asp
ENST00000498703.1:n.193_195delinsGAT
ENST00000610634.1:c.265_267delinsGAT	ENSP00000477517.1:p.His89Asp
NM_000314.5:c.367_369delinsGAT	NP_000305.3:p.His123Asp
NM_000314.6:c.367_369delinsGAT	NP_000305.3:p.His123Asp
NM_001304717.2:c.886_888delinsGAT	NP_001291646.2:p.His296Asp
NM_001304718.1:c.-384_-382delinsGAT	NP_001291647.1:n.-384_-382delinsGAT
XM_006717926.2:c.322_324delinsGAT	XP_006717989.1:p.His108Asp
XM_011539981.1:c.367_369delinsGAT	XP_011538283.1:p.His123Asp
XM_011539982.1:c.271_273delinsGAT	XP_011538284.1:p.His91Asp
XR_945789.1:n.1079_1081delinsGAT
XR_945790.1:n.1079_1081delinsGAT
XR_945791.1:n.1079_1081delinsGAT
NM_000314.7:c.367_369delinsGAT	NP_000305.3:p.His123Asp
NM_001304717.5:c.886_888delinsGAT	NP_001291646.4:p.His296Asp
NM_001304718.2:c.-384_-382delinsGAT	NP_001291647.1:n.-384_-382delinsGAT
NM_000314.8:c.367_369delinsGAT MANE Select	NP_000305.3:p.His123Asp