Canonical Allele Identifier: CA891834632

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960924_87960926delinsGAT , CM000672.2:g.87960924_87960926delinsGAT	GRCh38
NC_000010.10:g.89720681_89720683delinsGAT , CM000672.1:g.89720681_89720683delinsGAT	GRCh37
NC_000010.9:g.89710661_89710663delinsGAT	NCBI36
NG_007466.2:g.102486_102488delinsGAT , LRG_311:g.102486_102488delinsGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.925_927delinsGAT	ENSP00000514759.2:p.Phe309Asp
ENST00000710265.1:c.832_834delinsGAT	ENSP00000518161.1:p.Phe278Asp
ENST00000472832.3:c.832_834delinsGAT	ENSP00000483066.2:p.Phe278Asp
ENST00000688158.2:n.1567_1569delinsGAT
ENST00000688922.2:c.*662_*664delinsGAT	ENSP00000508742.2:n.*662_*664delinsGAT
ENST00000700021.1:c.787_789delinsGAT	ENSP00000514757.1:p.Phe263Asp
ENST00000700022.1:c.*171_*173delinsGAT	ENSP00000514758.1:n.*171_*173delinsGAT
ENST00000700023.1:n.1990_1992delinsGAT
ENST00000700024.1:n.2224_2226delinsGAT
ENST00000700025.1:n.1601_1603delinsGAT
ENST00000700026.1:n.469_471delinsGAT
ENST00000700029.1:c.759_761delinsGAT
ENST00000706954.1:c.832_834delinsGAT	ENSP00000516674.1:p.Phe278Asp
ENST00000706955.1:c.*867_*869delinsGAT	ENSP00000516675.1:n.*867_*869delinsGAT
ENST00000686459.1:c.*418_*420delinsGAT	ENSP00000508909.1:n.*418_*420delinsGAT
ENST00000688158.1:c.*943_*945delinsGAT	ENSP00000509254.1:n.*943_*945delinsGAT
ENST00000688308.1:c.832_834delinsGAT	ENSP00000508752.1:p.Phe278Asp
ENST00000688922.1:c.753_755delinsGAT
ENST00000693560.1:c.1351_1353delinsGAT	ENSP00000509861.1:p.Phe451Asp
ENST00000371953.8:c.832_834delinsGAT MANE Select	ENSP00000361021.3:p.Phe278Asp
ENST00000371953.7:c.832_834delinsGAT	ENSP00000361021.3:p.Phe278Asp
ENST00000472832.2:c.259_261delinsGAT	ENSP00000483066.1:p.Phe87Asp
NM_000314.5:c.832_834delinsGAT	NP_000305.3:p.Phe278Asp
NM_000314.6:c.832_834delinsGAT	NP_000305.3:p.Phe278Asp
NM_001304717.2:c.1351_1353delinsGAT	NP_001291646.2:p.Phe451Asp
NM_001304718.1:c.241_243delinsGAT	NP_001291647.1:p.Phe81Asp
XM_006717926.2:c.787_789delinsGAT	XP_006717989.1:p.Phe263Asp
XM_011539981.1:c.832_834delinsGAT	XP_011538283.1:p.Phe278Asp
XM_011539982.1:c.736_738delinsGAT	XP_011538284.1:p.Phe246Asp
XR_945791.1:n.1402_1404delinsGAT
NM_000314.7:c.832_834delinsGAT	NP_000305.3:p.Phe278Asp
NM_001304717.5:c.1351_1353delinsGAT	NP_001291646.4:p.Phe451Asp
NM_001304718.2:c.241_243delinsGAT	NP_001291647.1:p.Phe81Asp
NM_000314.8:c.832_834delinsGAT MANE Select	NP_000305.3:p.Phe278Asp