Canonical Allele Identifier: CA891838710

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952139_87952141delinsGAA , CM000672.2:g.87952139_87952141delinsGAA	GRCh38
NC_000010.10:g.89711896_89711898delinsGAA , CM000672.1:g.89711896_89711898delinsGAA	GRCh37
NC_000010.9:g.89701876_89701878delinsGAA	NCBI36
NG_007466.2:g.93701_93703delinsGAA , LRG_311:g.93701_93703delinsGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.514_516delinsGAA	ENSP00000514759.2:p.Arg172Glu
ENST00000710265.1:c.514_516delinsGAA	ENSP00000518161.1:p.Arg172Glu
ENST00000472832.3:c.514_516delinsGAA	ENSP00000483066.2:p.Arg172Glu
ENST00000688158.2:n.1249_1251delinsGAA
ENST00000688922.2:c.*344_*346delinsGAA	ENSP00000508742.2:n.*344_*346delinsGAA
ENST00000700021.1:c.469_471delinsGAA	ENSP00000514757.1:p.Arg157Glu
ENST00000700022.1:c.493-5714_493-5712delinsGAA	ENSP00000514758.1:n.493-5714_493-5712delinsGAA
ENST00000700023.1:n.1672_1674delinsGAA
ENST00000700024.1:n.1906_1908delinsGAA
ENST00000700025.1:n.1283_1285delinsGAA
ENST00000700029.1:c.348_350delinsGAA
ENST00000706954.1:c.514_516delinsGAA	ENSP00000516674.1:p.Arg172Glu
ENST00000706955.1:c.*549_*551delinsGAA	ENSP00000516675.1:n.*549_*551delinsGAA
ENST00000686459.1:c.*100_*102delinsGAA	ENSP00000508909.1:n.*100_*102delinsGAA
ENST00000688158.1:c.*625_*627delinsGAA	ENSP00000509254.1:n.*625_*627delinsGAA
ENST00000688308.1:c.514_516delinsGAA	ENSP00000508752.1:p.Arg172Glu
ENST00000688922.1:c.435_437delinsGAA
ENST00000693560.1:c.1033_1035delinsGAA	ENSP00000509861.1:p.Arg345Glu
ENST00000371953.8:c.514_516delinsGAA MANE Select	ENSP00000361021.3:p.Arg172Glu
ENST00000371953.7:c.514_516delinsGAA	ENSP00000361021.3:p.Arg172Glu
NM_000314.5:c.514_516delinsGAA	NP_000305.3:p.Arg172Glu
NM_000314.6:c.514_516delinsGAA	NP_000305.3:p.Arg172Glu
NM_001304717.2:c.1033_1035delinsGAA	NP_001291646.2:p.Arg345Glu
NM_001304718.1:c.-78_-76delinsGAA	NP_001291647.1:n.-78_-76delinsGAA
XM_006717926.2:c.469_471delinsGAA	XP_006717989.1:p.Arg157Glu
XM_011539981.1:c.514_516delinsGAA	XP_011538283.1:p.Arg172Glu
XM_011539982.1:c.418_420delinsGAA	XP_011538284.1:p.Arg140Glu
XR_945789.1:n.1385_1387delinsGAA
XR_945790.1:n.1502_1504delinsGAA
XR_945791.1:n.1205-5714_1205-5712delinsGAA
NM_000314.7:c.514_516delinsGAA	NP_000305.3:p.Arg172Glu
NM_001304717.5:c.1033_1035delinsGAA	NP_001291646.4:p.Arg345Glu
NM_001304718.2:c.-78_-76delinsGAA	NP_001291647.1:n.-78_-76delinsGAA
NM_000314.8:c.514_516delinsGAA MANE Select	NP_000305.3:p.Arg172Glu