Canonical Allele Identifier: CA891837312

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965336_87965337delinsAA , CM000672.2:g.87965336_87965337delinsAA	GRCh38
NC_000010.10:g.89725093_89725094delinsAA , CM000672.1:g.89725093_89725094delinsAA	GRCh37
NC_000010.9:g.89715073_89715074delinsAA	NCBI36
NG_007466.2:g.106898_106899delinsAA , LRG_311:g.106898_106899delinsAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1169_1170delinsAA	ENSP00000514759.2:p.Ala390Glu
ENST00000710265.1:c.*105_*106delinsAA	ENSP00000518161.1:n.*105_*106delinsAA
ENST00000688158.2:n.1811_1812delinsAA
ENST00000688922.2:c.*906_*907delinsAA	ENSP00000508742.2:n.*906_*907delinsAA
ENST00000700021.1:c.1031_1032delinsAA	ENSP00000514757.1:p.Ala344Glu
ENST00000700022.1:c.*415_*416delinsAA	ENSP00000514758.1:n.*415_*416delinsAA
ENST00000700023.1:n.2234_2235delinsAA
ENST00000700024.1:n.2468_2469delinsAA
ENST00000706954.1:c.1076_1077delinsAA	ENSP00000516674.1:p.Ala359Glu
ENST00000706955.1:c.*1111_*1112delinsAA	ENSP00000516675.1:n.*1111_*1112delinsAA
ENST00000686459.1:c.*662_*663delinsAA	ENSP00000508909.1:n.*662_*663delinsAA
ENST00000688158.1:c.*1187_*1188delinsAA	ENSP00000509254.1:n.*1187_*1188delinsAA
ENST00000688308.1:c.1076_1077delinsAA	ENSP00000508752.1:p.Ala359Glu
ENST00000688922.1:c.997_998delinsAA
ENST00000693560.1:c.1595_1596delinsAA	ENSP00000509861.1:p.Ala532Glu
ENST00000371953.8:c.1076_1077delinsAA MANE Select	ENSP00000361021.3:p.Ala359Glu
ENST00000371953.7:c.1076_1077delinsAA	ENSP00000361021.3:p.Ala359Glu
NM_000314.5:c.1076_1077delinsAA	NP_000305.3:p.Ala359Glu
NM_000314.6:c.1076_1077delinsAA	NP_000305.3:p.Ala359Glu
NM_001304717.2:c.1595_1596delinsAA	NP_001291646.2:p.Ala532Glu
NM_001304718.1:c.485_486delinsAA	NP_001291647.1:p.Ala162Glu
XM_006717926.2:c.1031_1032delinsAA	XP_006717989.1:p.Ala344Glu
XM_011539982.1:c.980_981delinsAA	XP_011538284.1:p.Ala327Glu
XR_945791.1:n.1646_1647delinsAA
NM_000314.7:c.1076_1077delinsAA	NP_000305.3:p.Ala359Glu
NM_001304717.5:c.1595_1596delinsAA	NP_001291646.4:p.Ala532Glu
NM_001304718.2:c.485_486delinsAA	NP_001291647.1:p.Ala162Glu
NM_000314.8:c.1076_1077delinsAA MANE Select	NP_000305.3:p.Ala359Glu