Canonical Allele Identifier: CA891834639

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960924_87960926delinsCAA , CM000672.2:g.87960924_87960926delinsCAA	GRCh38
NC_000010.10:g.89720681_89720683delinsCAA , CM000672.1:g.89720681_89720683delinsCAA	GRCh37
NC_000010.9:g.89710661_89710663delinsCAA	NCBI36
NG_007466.2:g.102486_102488delinsCAA , LRG_311:g.102486_102488delinsCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.925_927delinsCAA	ENSP00000514759.2:p.Phe309Gln
ENST00000710265.1:c.832_834delinsCAA	ENSP00000518161.1:p.Phe278Gln
ENST00000472832.3:c.832_834delinsCAA	ENSP00000483066.2:p.Phe278Gln
ENST00000688158.2:n.1567_1569delinsCAA
ENST00000688922.2:c.*662_*664delinsCAA	ENSP00000508742.2:n.*662_*664delinsCAA
ENST00000700021.1:c.787_789delinsCAA	ENSP00000514757.1:p.Phe263Gln
ENST00000700022.1:c.*171_*173delinsCAA	ENSP00000514758.1:n.*171_*173delinsCAA
ENST00000700023.1:n.1990_1992delinsCAA
ENST00000700024.1:n.2224_2226delinsCAA
ENST00000700025.1:n.1601_1603delinsCAA
ENST00000700026.1:n.469_471delinsCAA
ENST00000700029.1:c.759_761delinsCAA
ENST00000706954.1:c.832_834delinsCAA	ENSP00000516674.1:p.Phe278Gln
ENST00000706955.1:c.*867_*869delinsCAA	ENSP00000516675.1:n.*867_*869delinsCAA
ENST00000686459.1:c.*418_*420delinsCAA	ENSP00000508909.1:n.*418_*420delinsCAA
ENST00000688158.1:c.*943_*945delinsCAA	ENSP00000509254.1:n.*943_*945delinsCAA
ENST00000688308.1:c.832_834delinsCAA	ENSP00000508752.1:p.Phe278Gln
ENST00000688922.1:c.753_755delinsCAA
ENST00000693560.1:c.1351_1353delinsCAA	ENSP00000509861.1:p.Phe451Gln
ENST00000371953.8:c.832_834delinsCAA MANE Select	ENSP00000361021.3:p.Phe278Gln
ENST00000371953.7:c.832_834delinsCAA	ENSP00000361021.3:p.Phe278Gln
ENST00000472832.2:c.259_261delinsCAA	ENSP00000483066.1:p.Phe87Gln
NM_000314.5:c.832_834delinsCAA	NP_000305.3:p.Phe278Gln
NM_000314.6:c.832_834delinsCAA	NP_000305.3:p.Phe278Gln
NM_001304717.2:c.1351_1353delinsCAA	NP_001291646.2:p.Phe451Gln
NM_001304718.1:c.241_243delinsCAA	NP_001291647.1:p.Phe81Gln
XM_006717926.2:c.787_789delinsCAA	XP_006717989.1:p.Phe263Gln
XM_011539981.1:c.832_834delinsCAA	XP_011538283.1:p.Phe278Gln
XM_011539982.1:c.736_738delinsCAA	XP_011538284.1:p.Phe246Gln
XR_945791.1:n.1402_1404delinsCAA
NM_000314.7:c.832_834delinsCAA	NP_000305.3:p.Phe278Gln
NM_001304717.5:c.1351_1353delinsCAA	NP_001291646.4:p.Phe451Gln
NM_001304718.2:c.241_243delinsCAA	NP_001291647.1:p.Phe81Gln
NM_000314.8:c.832_834delinsCAA MANE Select	NP_000305.3:p.Phe278Gln