Canonical Allele Identifier: CA891841681

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965440_87965441delinsCG , CM000672.2:g.87965440_87965441delinsCG	GRCh38
NC_000010.10:g.89725197_89725198delinsCG , CM000672.1:g.89725197_89725198delinsCG	GRCh37
NC_000010.9:g.89715177_89715178delinsCG	NCBI36
NG_007466.2:g.107002_107003delinsCG , LRG_311:g.107002_107003delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1273_1274delinsCG	ENSP00000514759.2:p.Glu425Arg
ENST00000710265.1:c.*209_*210delinsCG	ENSP00000518161.1:n.*209_*210delinsCG
ENST00000688158.2:n.1915_1916delinsCG
ENST00000688922.2:c.*1010_*1011delinsCG	ENSP00000508742.2:n.*1010_*1011delinsCG
ENST00000700021.1:c.1135_1136delinsCG	ENSP00000514757.1:p.Glu379Arg
ENST00000700022.1:c.*519_*520delinsCG	ENSP00000514758.1:n.*519_*520delinsCG
ENST00000700023.1:n.2338_2339delinsCG
ENST00000700024.1:n.2572_2573delinsCG
ENST00000706954.1:c.1180_1181delinsCG	ENSP00000516674.1:p.Glu394Arg
ENST00000706955.1:c.*1215_*1216delinsCG	ENSP00000516675.1:n.*1215_*1216delinsCG
ENST00000686459.1:c.*766_*767delinsCG	ENSP00000508909.1:n.*766_*767delinsCG
ENST00000688158.1:c.*1291_*1292delinsCG	ENSP00000509254.1:n.*1291_*1292delinsCG
ENST00000688308.1:c.1180_1181delinsCG	ENSP00000508752.1:p.Glu394Arg
ENST00000688922.1:c.1101_1102delinsCG
ENST00000693560.1:c.1699_1700delinsCG	ENSP00000509861.1:p.Glu567Arg
ENST00000371953.8:c.1180_1181delinsCG MANE Select	ENSP00000361021.3:p.Glu394Arg
ENST00000371953.7:c.1180_1181delinsCG	ENSP00000361021.3:p.Glu394Arg
NM_000314.5:c.1180_1181delinsCG	NP_000305.3:p.Glu394Arg
NM_000314.6:c.1180_1181delinsCG	NP_000305.3:p.Glu394Arg
NM_001304717.2:c.1699_1700delinsCG	NP_001291646.2:p.Glu567Arg
NM_001304718.1:c.589_590delinsCG	NP_001291647.1:p.Glu197Arg
XM_006717926.2:c.1135_1136delinsCG	XP_006717989.1:p.Glu379Arg
XM_011539982.1:c.1084_1085delinsCG	XP_011538284.1:p.Glu362Arg
XR_945791.1:n.1750_1751delinsCG
NM_000314.7:c.1180_1181delinsCG	NP_000305.3:p.Glu394Arg
NM_001304717.5:c.1699_1700delinsCG	NP_001291646.4:p.Glu567Arg
NM_001304718.2:c.589_590delinsCG	NP_001291647.1:p.Glu197Arg
NM_000314.8:c.1180_1181delinsCG MANE Select	NP_000305.3:p.Glu394Arg