Canonical Allele Identifier: CA891834647

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960924_87960926delinsGTT , CM000672.2:g.87960924_87960926delinsGTT	GRCh38
NC_000010.10:g.89720681_89720683delinsGTT , CM000672.1:g.89720681_89720683delinsGTT	GRCh37
NC_000010.9:g.89710661_89710663delinsGTT	NCBI36
NG_007466.2:g.102486_102488delinsGTT , LRG_311:g.102486_102488delinsGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.925_927delinsGTT	ENSP00000514759.2:p.Phe309Val
ENST00000710265.1:c.832_834delinsGTT	ENSP00000518161.1:p.Phe278Val
ENST00000472832.3:c.832_834delinsGTT	ENSP00000483066.2:p.Phe278Val
ENST00000688158.2:n.1567_1569delinsGTT
ENST00000688922.2:c.*662_*664delinsGTT	ENSP00000508742.2:n.*662_*664delinsGTT
ENST00000700021.1:c.787_789delinsGTT	ENSP00000514757.1:p.Phe263Val
ENST00000700022.1:c.*171_*173delinsGTT	ENSP00000514758.1:n.*171_*173delinsGTT
ENST00000700023.1:n.1990_1992delinsGTT
ENST00000700024.1:n.2224_2226delinsGTT
ENST00000700025.1:n.1601_1603delinsGTT
ENST00000700026.1:n.469_471delinsGTT
ENST00000700029.1:c.759_761delinsGTT
ENST00000706954.1:c.832_834delinsGTT	ENSP00000516674.1:p.Phe278Val
ENST00000706955.1:c.*867_*869delinsGTT	ENSP00000516675.1:n.*867_*869delinsGTT
ENST00000686459.1:c.*418_*420delinsGTT	ENSP00000508909.1:n.*418_*420delinsGTT
ENST00000688158.1:c.*943_*945delinsGTT	ENSP00000509254.1:n.*943_*945delinsGTT
ENST00000688308.1:c.832_834delinsGTT	ENSP00000508752.1:p.Phe278Val
ENST00000688922.1:c.753_755delinsGTT
ENST00000693560.1:c.1351_1353delinsGTT	ENSP00000509861.1:p.Phe451Val
ENST00000371953.8:c.832_834delinsGTT MANE Select	ENSP00000361021.3:p.Phe278Val
ENST00000371953.7:c.832_834delinsGTT	ENSP00000361021.3:p.Phe278Val
ENST00000472832.2:c.259_261delinsGTT	ENSP00000483066.1:p.Phe87Val
NM_000314.5:c.832_834delinsGTT	NP_000305.3:p.Phe278Val
NM_000314.6:c.832_834delinsGTT	NP_000305.3:p.Phe278Val
NM_001304717.2:c.1351_1353delinsGTT	NP_001291646.2:p.Phe451Val
NM_001304718.1:c.241_243delinsGTT	NP_001291647.1:p.Phe81Val
XM_006717926.2:c.787_789delinsGTT	XP_006717989.1:p.Phe263Val
XM_011539981.1:c.832_834delinsGTT	XP_011538283.1:p.Phe278Val
XM_011539982.1:c.736_738delinsGTT	XP_011538284.1:p.Phe246Val
XR_945791.1:n.1402_1404delinsGTT
NM_000314.7:c.832_834delinsGTT	NP_000305.3:p.Phe278Val
NM_001304717.5:c.1351_1353delinsGTT	NP_001291646.4:p.Phe451Val
NM_001304718.2:c.241_243delinsGTT	NP_001291647.1:p.Phe81Val
NM_000314.8:c.832_834delinsGTT MANE Select	NP_000305.3:p.Phe278Val