Canonical Allele Identifier: CA891841682

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965440_87965441delinsCC , CM000672.2:g.87965440_87965441delinsCC	GRCh38
NC_000010.10:g.89725197_89725198delinsCC , CM000672.1:g.89725197_89725198delinsCC	GRCh37
NC_000010.9:g.89715177_89715178delinsCC	NCBI36
NG_007466.2:g.107002_107003delinsCC , LRG_311:g.107002_107003delinsCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1273_1274delinsCC	ENSP00000514759.2:p.Glu425Pro
ENST00000710265.1:c.*209_*210delinsCC	ENSP00000518161.1:n.*209_*210delinsCC
ENST00000688158.2:n.1915_1916delinsCC
ENST00000688922.2:c.*1010_*1011delinsCC	ENSP00000508742.2:n.*1010_*1011delinsCC
ENST00000700021.1:c.1135_1136delinsCC	ENSP00000514757.1:p.Glu379Pro
ENST00000700022.1:c.*519_*520delinsCC	ENSP00000514758.1:n.*519_*520delinsCC
ENST00000700023.1:n.2338_2339delinsCC
ENST00000700024.1:n.2572_2573delinsCC
ENST00000706954.1:c.1180_1181delinsCC	ENSP00000516674.1:p.Glu394Pro
ENST00000706955.1:c.*1215_*1216delinsCC	ENSP00000516675.1:n.*1215_*1216delinsCC
ENST00000686459.1:c.*766_*767delinsCC	ENSP00000508909.1:n.*766_*767delinsCC
ENST00000688158.1:c.*1291_*1292delinsCC	ENSP00000509254.1:n.*1291_*1292delinsCC
ENST00000688308.1:c.1180_1181delinsCC	ENSP00000508752.1:p.Glu394Pro
ENST00000688922.1:c.1101_1102delinsCC
ENST00000693560.1:c.1699_1700delinsCC	ENSP00000509861.1:p.Glu567Pro
ENST00000371953.8:c.1180_1181delinsCC MANE Select	ENSP00000361021.3:p.Glu394Pro
ENST00000371953.7:c.1180_1181delinsCC	ENSP00000361021.3:p.Glu394Pro
NM_000314.5:c.1180_1181delinsCC	NP_000305.3:p.Glu394Pro
NM_000314.6:c.1180_1181delinsCC	NP_000305.3:p.Glu394Pro
NM_001304717.2:c.1699_1700delinsCC	NP_001291646.2:p.Glu567Pro
NM_001304718.1:c.589_590delinsCC	NP_001291647.1:p.Glu197Pro
XM_006717926.2:c.1135_1136delinsCC	XP_006717989.1:p.Glu379Pro
XM_011539982.1:c.1084_1085delinsCC	XP_011538284.1:p.Glu362Pro
XR_945791.1:n.1750_1751delinsCC
NM_000314.7:c.1180_1181delinsCC	NP_000305.3:p.Glu394Pro
NM_001304717.5:c.1699_1700delinsCC	NP_001291646.4:p.Glu567Pro
NM_001304718.2:c.589_590delinsCC	NP_001291647.1:p.Glu197Pro
NM_000314.8:c.1180_1181delinsCC MANE Select	NP_000305.3:p.Glu394Pro