Canonical Allele Identifier: CA891837540

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87933135_87933136delinsTG , CM000672.2:g.87933135_87933136delinsTG	GRCh38
NC_000010.10:g.89692892_89692893delinsTG , CM000672.1:g.89692892_89692893delinsTG	GRCh37
NC_000010.9:g.89682872_89682873delinsTG	NCBI36
NG_007466.2:g.74697_74698delinsTG , LRG_311:g.74697_74698delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.376_377delinsTG	ENSP00000514759.2:p.Ala126Cys
ENST00000710265.1:c.376_377delinsTG	ENSP00000518161.1:p.Ala126Cys
ENST00000472832.3:c.376_377delinsTG	ENSP00000483066.2:p.Ala126Cys
ENST00000688158.2:n.1111_1112delinsTG
ENST00000688922.2:c.*206_*207delinsTG	ENSP00000508742.2:n.*206_*207delinsTG
ENST00000700021.1:c.331_332delinsTG	ENSP00000514757.1:p.Ala111Cys
ENST00000700022.1:c.376_377delinsTG	ENSP00000514758.1:p.Ala126Cys
ENST00000700029.1:c.210_211delinsTG
ENST00000706954.1:c.376_377delinsTG	ENSP00000516674.1:p.Ala126Cys
ENST00000706955.1:c.*411_*412delinsTG	ENSP00000516675.1:n.*411_*412delinsTG
ENST00000686459.1:c.376_377delinsTG	ENSP00000508909.1:p.Ala126Cys
ENST00000688158.1:c.*487_*488delinsTG	ENSP00000509254.1:n.*487_*488delinsTG
ENST00000688308.1:c.376_377delinsTG	ENSP00000508752.1:p.Ala126Cys
ENST00000688922.1:c.297_298delinsTG
ENST00000693560.1:c.895_896delinsTG	ENSP00000509861.1:p.Ala299Cys
ENST00000371953.8:c.376_377delinsTG MANE Select	ENSP00000361021.3:p.Ala126Cys
ENST00000371953.7:c.376_377delinsTG	ENSP00000361021.3:p.Ala126Cys
ENST00000498703.1:n.202_203delinsTG
ENST00000610634.1:c.274_275delinsTG	ENSP00000477517.1:p.Ala92Cys
NM_000314.5:c.376_377delinsTG	NP_000305.3:p.Ala126Cys
NM_000314.6:c.376_377delinsTG	NP_000305.3:p.Ala126Cys
NM_001304717.2:c.895_896delinsTG	NP_001291646.2:p.Ala299Cys
NM_001304718.1:c.-375_-374delinsTG	NP_001291647.1:n.-375_-374delinsTG
XM_006717926.2:c.331_332delinsTG	XP_006717989.1:p.Ala111Cys
XM_011539981.1:c.376_377delinsTG	XP_011538283.1:p.Ala126Cys
XM_011539982.1:c.280_281delinsTG	XP_011538284.1:p.Ala94Cys
XR_945789.1:n.1088_1089delinsTG
XR_945790.1:n.1088_1089delinsTG
XR_945791.1:n.1088_1089delinsTG
NM_000314.7:c.376_377delinsTG	NP_000305.3:p.Ala126Cys
NM_001304717.5:c.895_896delinsTG	NP_001291646.4:p.Ala299Cys
NM_001304718.2:c.-375_-374delinsTG	NP_001291647.1:n.-375_-374delinsTG
NM_000314.8:c.376_377delinsTG MANE Select	NP_000305.3:p.Ala126Cys