Canonical Allele Identifier: CA891837305

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87933117_87933119delinsTCT , CM000672.2:g.87933117_87933119delinsTCT	GRCh38
NC_000010.10:g.89692874_89692876delinsTCT , CM000672.1:g.89692874_89692876delinsTCT	GRCh37
NC_000010.9:g.89682854_89682856delinsTCT	NCBI36
NG_007466.2:g.74679_74681delinsTCT , LRG_311:g.74679_74681delinsTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.358_360delinsTCT	ENSP00000514759.2:p.Ala120Ser
ENST00000710265.1:c.358_360delinsTCT	ENSP00000518161.1:p.Ala120Ser
ENST00000472832.3:c.358_360delinsTCT	ENSP00000483066.2:p.Ala120Ser
ENST00000688158.2:n.1093_1095delinsTCT
ENST00000688922.2:c.*188_*190delinsTCT	ENSP00000508742.2:n.*188_*190delinsTCT
ENST00000700021.1:c.313_315delinsTCT	ENSP00000514757.1:p.Ala105Ser
ENST00000700022.1:c.358_360delinsTCT	ENSP00000514758.1:p.Ala120Ser
ENST00000700029.1:c.192_194delinsTCT
ENST00000706954.1:c.358_360delinsTCT	ENSP00000516674.1:p.Ala120Ser
ENST00000706955.1:c.*393_*395delinsTCT	ENSP00000516675.1:n.*393_*395delinsTCT
ENST00000686459.1:c.358_360delinsTCT	ENSP00000508909.1:p.Ala120Ser
ENST00000688158.1:c.*469_*471delinsTCT	ENSP00000509254.1:n.*469_*471delinsTCT
ENST00000688308.1:c.358_360delinsTCT	ENSP00000508752.1:p.Ala120Ser
ENST00000688922.1:c.279_281delinsTCT
ENST00000693560.1:c.877_879delinsTCT	ENSP00000509861.1:p.Ala293Ser
ENST00000371953.8:c.358_360delinsTCT MANE Select	ENSP00000361021.3:p.Ala120Ser
ENST00000371953.7:c.358_360delinsTCT	ENSP00000361021.3:p.Ala120Ser
ENST00000498703.1:n.184_186delinsTCT
ENST00000610634.1:c.256_258delinsTCT	ENSP00000477517.1:p.Ala86Ser
NM_000314.5:c.358_360delinsTCT	NP_000305.3:p.Ala120Ser
NM_000314.6:c.358_360delinsTCT	NP_000305.3:p.Ala120Ser
NM_001304717.2:c.877_879delinsTCT	NP_001291646.2:p.Ala293Ser
NM_001304718.1:c.-393_-391delinsTCT	NP_001291647.1:n.-393_-391delinsTCT
XM_006717926.2:c.313_315delinsTCT	XP_006717989.1:p.Ala105Ser
XM_011539981.1:c.358_360delinsTCT	XP_011538283.1:p.Ala120Ser
XM_011539982.1:c.262_264delinsTCT	XP_011538284.1:p.Ala88Ser
XR_945789.1:n.1070_1072delinsTCT
XR_945790.1:n.1070_1072delinsTCT
XR_945791.1:n.1070_1072delinsTCT
NM_000314.7:c.358_360delinsTCT	NP_000305.3:p.Ala120Ser
NM_001304717.5:c.877_879delinsTCT	NP_001291646.4:p.Ala293Ser
NM_001304718.2:c.-393_-391delinsTCT	NP_001291647.1:n.-393_-391delinsTCT
NM_000314.8:c.358_360delinsTCT MANE Select	NP_000305.3:p.Ala120Ser