Canonical Allele Identifier: CA891841654

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965422_87965423delinsAC , CM000672.2:g.87965422_87965423delinsAC	GRCh38
NC_000010.10:g.89725179_89725180delinsAC , CM000672.1:g.89725179_89725180delinsAC	GRCh37
NC_000010.9:g.89715159_89715160delinsAC	NCBI36
NG_007466.2:g.106984_106985delinsAC , LRG_311:g.106984_106985delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1255_1256delinsAC	ENSP00000514759.2:p.Glu419Thr
ENST00000710265.1:c.*191_*192delinsAC	ENSP00000518161.1:n.*191_*192delinsAC
ENST00000688158.2:n.1897_1898delinsAC
ENST00000688922.2:c.*992_*993delinsAC	ENSP00000508742.2:n.*992_*993delinsAC
ENST00000700021.1:c.1117_1118delinsAC	ENSP00000514757.1:p.Glu373Thr
ENST00000700022.1:c.*501_*502delinsAC	ENSP00000514758.1:n.*501_*502delinsAC
ENST00000700023.1:n.2320_2321delinsAC
ENST00000700024.1:n.2554_2555delinsAC
ENST00000706954.1:c.1162_1163delinsAC	ENSP00000516674.1:p.Glu388Thr
ENST00000706955.1:c.*1197_*1198delinsAC	ENSP00000516675.1:n.*1197_*1198delinsAC
ENST00000686459.1:c.*748_*749delinsAC	ENSP00000508909.1:n.*748_*749delinsAC
ENST00000688158.1:c.*1273_*1274delinsAC	ENSP00000509254.1:n.*1273_*1274delinsAC
ENST00000688308.1:c.1162_1163delinsAC	ENSP00000508752.1:p.Glu388Thr
ENST00000688922.1:c.1083_1084delinsAC
ENST00000693560.1:c.1681_1682delinsAC	ENSP00000509861.1:p.Glu561Thr
ENST00000371953.8:c.1162_1163delinsAC MANE Select	ENSP00000361021.3:p.Glu388Thr
ENST00000371953.7:c.1162_1163delinsAC	ENSP00000361021.3:p.Glu388Thr
NM_000314.5:c.1162_1163delinsAC	NP_000305.3:p.Glu388Thr
NM_000314.6:c.1162_1163delinsAC	NP_000305.3:p.Glu388Thr
NM_001304717.2:c.1681_1682delinsAC	NP_001291646.2:p.Glu561Thr
NM_001304718.1:c.571_572delinsAC	NP_001291647.1:p.Glu191Thr
XM_006717926.2:c.1117_1118delinsAC	XP_006717989.1:p.Glu373Thr
XM_011539982.1:c.1066_1067delinsAC	XP_011538284.1:p.Glu356Thr
XR_945791.1:n.1732_1733delinsAC
NM_000314.7:c.1162_1163delinsAC	NP_000305.3:p.Glu388Thr
NM_001304717.5:c.1681_1682delinsAC	NP_001291646.4:p.Glu561Thr
NM_001304718.2:c.571_572delinsAC	NP_001291647.1:p.Glu191Thr
NM_000314.8:c.1162_1163delinsAC MANE Select	NP_000305.3:p.Glu388Thr