Canonical Allele Identifier: CA891837420

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87933126_87933128delinsTAT , CM000672.2:g.87933126_87933128delinsTAT	GRCh38
NC_000010.10:g.89692883_89692885delinsTAT , CM000672.1:g.89692883_89692885delinsTAT	GRCh37
NC_000010.9:g.89682863_89682865delinsTAT	NCBI36
NG_007466.2:g.74688_74690delinsTAT , LRG_311:g.74688_74690delinsTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.367_369delinsTAT	ENSP00000514759.2:p.His123Tyr
ENST00000710265.1:c.367_369delinsTAT	ENSP00000518161.1:p.His123Tyr
ENST00000472832.3:c.367_369delinsTAT	ENSP00000483066.2:p.His123Tyr
ENST00000688158.2:n.1102_1104delinsTAT
ENST00000688922.2:c.*197_*199delinsTAT	ENSP00000508742.2:n.*197_*199delinsTAT
ENST00000700021.1:c.322_324delinsTAT	ENSP00000514757.1:p.His108Tyr
ENST00000700022.1:c.367_369delinsTAT	ENSP00000514758.1:p.His123Tyr
ENST00000700029.1:c.201_203delinsTAT
ENST00000706954.1:c.367_369delinsTAT	ENSP00000516674.1:p.His123Tyr
ENST00000706955.1:c.*402_*404delinsTAT	ENSP00000516675.1:n.*402_*404delinsTAT
ENST00000686459.1:c.367_369delinsTAT	ENSP00000508909.1:p.His123Tyr
ENST00000688158.1:c.*478_*480delinsTAT	ENSP00000509254.1:n.*478_*480delinsTAT
ENST00000688308.1:c.367_369delinsTAT	ENSP00000508752.1:p.His123Tyr
ENST00000688922.1:c.288_290delinsTAT
ENST00000693560.1:c.886_888delinsTAT	ENSP00000509861.1:p.His296Tyr
ENST00000371953.8:c.367_369delinsTAT MANE Select	ENSP00000361021.3:p.His123Tyr
ENST00000371953.7:c.367_369delinsTAT	ENSP00000361021.3:p.His123Tyr
ENST00000498703.1:n.193_195delinsTAT
ENST00000610634.1:c.265_267delinsTAT	ENSP00000477517.1:p.His89Tyr
NM_000314.5:c.367_369delinsTAT	NP_000305.3:p.His123Tyr
NM_000314.6:c.367_369delinsTAT	NP_000305.3:p.His123Tyr
NM_001304717.2:c.886_888delinsTAT	NP_001291646.2:p.His296Tyr
NM_001304718.1:c.-384_-382delinsTAT	NP_001291647.1:n.-384_-382delinsTAT
XM_006717926.2:c.322_324delinsTAT	XP_006717989.1:p.His108Tyr
XM_011539981.1:c.367_369delinsTAT	XP_011538283.1:p.His123Tyr
XM_011539982.1:c.271_273delinsTAT	XP_011538284.1:p.His91Tyr
XR_945789.1:n.1079_1081delinsTAT
XR_945790.1:n.1079_1081delinsTAT
XR_945791.1:n.1079_1081delinsTAT
NM_000314.7:c.367_369delinsTAT	NP_000305.3:p.His123Tyr
NM_001304717.5:c.886_888delinsTAT	NP_001291646.4:p.His296Tyr
NM_001304718.2:c.-384_-382delinsTAT	NP_001291647.1:n.-384_-382delinsTAT
NM_000314.8:c.367_369delinsTAT MANE Select	NP_000305.3:p.His123Tyr