Canonical Allele Identifier: CA891841680

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965440_87965441delinsTC , CM000672.2:g.87965440_87965441delinsTC	GRCh38
NC_000010.10:g.89725197_89725198delinsTC , CM000672.1:g.89725197_89725198delinsTC	GRCh37
NC_000010.9:g.89715177_89715178delinsTC	NCBI36
NG_007466.2:g.107002_107003delinsTC , LRG_311:g.107002_107003delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1273_1274delinsTC	ENSP00000514759.2:p.Glu425Ser
ENST00000710265.1:c.*209_*210delinsTC	ENSP00000518161.1:n.*209_*210delinsTC
ENST00000688158.2:n.1915_1916delinsTC
ENST00000688922.2:c.*1010_*1011delinsTC	ENSP00000508742.2:n.*1010_*1011delinsTC
ENST00000700021.1:c.1135_1136delinsTC	ENSP00000514757.1:p.Glu379Ser
ENST00000700022.1:c.*519_*520delinsTC	ENSP00000514758.1:n.*519_*520delinsTC
ENST00000700023.1:n.2338_2339delinsTC
ENST00000700024.1:n.2572_2573delinsTC
ENST00000706954.1:c.1180_1181delinsTC	ENSP00000516674.1:p.Glu394Ser
ENST00000706955.1:c.*1215_*1216delinsTC	ENSP00000516675.1:n.*1215_*1216delinsTC
ENST00000686459.1:c.*766_*767delinsTC	ENSP00000508909.1:n.*766_*767delinsTC
ENST00000688158.1:c.*1291_*1292delinsTC	ENSP00000509254.1:n.*1291_*1292delinsTC
ENST00000688308.1:c.1180_1181delinsTC	ENSP00000508752.1:p.Glu394Ser
ENST00000688922.1:c.1101_1102delinsTC
ENST00000693560.1:c.1699_1700delinsTC	ENSP00000509861.1:p.Glu567Ser
ENST00000371953.8:c.1180_1181delinsTC MANE Select	ENSP00000361021.3:p.Glu394Ser
ENST00000371953.7:c.1180_1181delinsTC	ENSP00000361021.3:p.Glu394Ser
NM_000314.5:c.1180_1181delinsTC	NP_000305.3:p.Glu394Ser
NM_000314.6:c.1180_1181delinsTC	NP_000305.3:p.Glu394Ser
NM_001304717.2:c.1699_1700delinsTC	NP_001291646.2:p.Glu567Ser
NM_001304718.1:c.589_590delinsTC	NP_001291647.1:p.Glu197Ser
XM_006717926.2:c.1135_1136delinsTC	XP_006717989.1:p.Glu379Ser
XM_011539982.1:c.1084_1085delinsTC	XP_011538284.1:p.Glu362Ser
XR_945791.1:n.1750_1751delinsTC
NM_000314.7:c.1180_1181delinsTC	NP_000305.3:p.Glu394Ser
NM_001304717.5:c.1699_1700delinsTC	NP_001291646.4:p.Glu567Ser
NM_001304718.2:c.589_590delinsTC	NP_001291647.1:p.Glu197Ser
NM_000314.8:c.1180_1181delinsTC MANE Select	NP_000305.3:p.Glu394Ser