Canonical Allele Identifier: CA891841397

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961095_87961096delinsGA , CM000672.2:g.87961095_87961096delinsGA	GRCh38
NC_000010.10:g.89720852_89720853delinsGA , CM000672.1:g.89720852_89720853delinsGA	GRCh37
NC_000010.9:g.89710832_89710833delinsGA	NCBI36
NG_007466.2:g.102657_102658delinsGA , LRG_311:g.102657_102658delinsGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.1096_1097delinsGA	ENSP00000514759.2:p.Arg366Glu
ENST00000710265.1:c.1003_1004delinsGA	ENSP00000518161.1:p.Arg335Glu
ENST00000472832.3:c.1003_1004delinsGA	ENSP00000483066.2:p.Arg335Glu
ENST00000688158.2:n.1738_1739delinsGA
ENST00000688922.2:c.*833_*834delinsGA	ENSP00000508742.2:n.*833_*834delinsGA
ENST00000700021.1:c.958_959delinsGA	ENSP00000514757.1:p.Arg320Glu
ENST00000700022.1:c.*342_*343delinsGA	ENSP00000514758.1:n.*342_*343delinsGA
ENST00000700023.1:n.2161_2162delinsGA
ENST00000700024.1:n.2395_2396delinsGA
ENST00000700025.1:n.1772_1773delinsGA
ENST00000700026.1:n.640_641delinsGA
ENST00000706954.1:c.1003_1004delinsGA	ENSP00000516674.1:p.Arg335Glu
ENST00000706955.1:c.*1038_*1039delinsGA	ENSP00000516675.1:n.*1038_*1039delinsGA
ENST00000686459.1:c.*589_*590delinsGA	ENSP00000508909.1:n.*589_*590delinsGA
ENST00000688158.1:c.*1114_*1115delinsGA	ENSP00000509254.1:n.*1114_*1115delinsGA
ENST00000688308.1:c.1003_1004delinsGA	ENSP00000508752.1:p.Arg335Glu
ENST00000688922.1:c.924_925delinsGA
ENST00000693560.1:c.1522_1523delinsGA	ENSP00000509861.1:p.Arg508Glu
ENST00000371953.8:c.1003_1004delinsGA MANE Select	ENSP00000361021.3:p.Arg335Glu
ENST00000371953.7:c.1003_1004delinsGA	ENSP00000361021.3:p.Arg335Glu
ENST00000472832.2:c.430_431delinsGA	ENSP00000483066.1:p.Arg144Glu
NM_000314.5:c.1003_1004delinsGA	NP_000305.3:p.Arg335Glu
NM_000314.6:c.1003_1004delinsGA	NP_000305.3:p.Arg335Glu
NM_001304717.2:c.1522_1523delinsGA	NP_001291646.2:p.Arg508Glu
NM_001304718.1:c.412_413delinsGA	NP_001291647.1:p.Arg138Glu
XM_006717926.2:c.958_959delinsGA	XP_006717989.1:p.Arg320Glu
XM_011539981.1:c.1003_1004delinsGA	XP_011538283.1:p.Arg335Glu
XM_011539982.1:c.907_908delinsGA	XP_011538284.1:p.Arg303Glu
XR_945791.1:n.1573_1574delinsGA
NM_000314.7:c.1003_1004delinsGA	NP_000305.3:p.Arg335Glu
NM_001304717.5:c.1522_1523delinsGA	NP_001291646.4:p.Arg508Glu
NM_001304718.2:c.412_413delinsGA	NP_001291647.1:p.Arg138Glu
NM_000314.8:c.1003_1004delinsGA MANE Select	NP_000305.3:p.Arg335Glu