Canonical Allele Identifier: CA891836939

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961101_87961102delinsGC , CM000672.2:g.87961101_87961102delinsGC	GRCh38
NC_000010.10:g.89720858_89720859delinsGC , CM000672.1:g.89720858_89720859delinsGC	GRCh37
NC_000010.9:g.89710838_89710839delinsGC	NCBI36
NG_007466.2:g.102663_102664delinsGC , LRG_311:g.102663_102664delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1102_1103delinsGC	ENSP00000514759.2:p.Phe368Ala
ENST00000710265.1:c.1009_1010delinsGC	ENSP00000518161.1:p.Phe337Ala
ENST00000472832.3:c.1009_1010delinsGC	ENSP00000483066.2:p.Phe337Ala
ENST00000688158.2:n.1744_1745delinsGC
ENST00000688922.2:c.*839_*840delinsGC	ENSP00000508742.2:n.*839_*840delinsGC
ENST00000700021.1:c.964_965delinsGC	ENSP00000514757.1:p.Phe322Ala
ENST00000700022.1:c.*348_*349delinsGC	ENSP00000514758.1:n.*348_*349delinsGC
ENST00000700023.1:n.2167_2168delinsGC
ENST00000700024.1:n.2401_2402delinsGC
ENST00000700025.1:n.1778_1779delinsGC
ENST00000700026.1:n.646_647delinsGC
ENST00000706954.1:c.1009_1010delinsGC	ENSP00000516674.1:p.Phe337Ala
ENST00000706955.1:c.*1044_*1045delinsGC	ENSP00000516675.1:n.*1044_*1045delinsGC
ENST00000686459.1:c.*595_*596delinsGC	ENSP00000508909.1:n.*595_*596delinsGC
ENST00000688158.1:c.*1120_*1121delinsGC	ENSP00000509254.1:n.*1120_*1121delinsGC
ENST00000688308.1:c.1009_1010delinsGC	ENSP00000508752.1:p.Phe337Ala
ENST00000688922.1:c.930_931delinsGC
ENST00000693560.1:c.1528_1529delinsGC	ENSP00000509861.1:p.Phe510Ala
ENST00000371953.8:c.1009_1010delinsGC MANE Select	ENSP00000361021.3:p.Phe337Ala
ENST00000371953.7:c.1009_1010delinsGC	ENSP00000361021.3:p.Phe337Ala
ENST00000472832.2:c.436_437delinsGC	ENSP00000483066.1:p.Phe146Ala
NM_000314.5:c.1009_1010delinsGC	NP_000305.3:p.Phe337Ala
NM_000314.6:c.1009_1010delinsGC	NP_000305.3:p.Phe337Ala
NM_001304717.2:c.1528_1529delinsGC	NP_001291646.2:p.Phe510Ala
NM_001304718.1:c.418_419delinsGC	NP_001291647.1:p.Phe140Ala
XM_006717926.2:c.964_965delinsGC	XP_006717989.1:p.Phe322Ala
XM_011539981.1:c.1009_1010delinsGC	XP_011538283.1:p.Phe337Ala
XM_011539982.1:c.913_914delinsGC	XP_011538284.1:p.Phe305Ala
XR_945791.1:n.1579_1580delinsGC
NM_000314.7:c.1009_1010delinsGC	NP_000305.3:p.Phe337Ala
NM_001304717.5:c.1528_1529delinsGC	NP_001291646.4:p.Phe510Ala
NM_001304718.2:c.418_419delinsGC	NP_001291647.1:p.Phe140Ala
NM_000314.8:c.1009_1010delinsGC MANE Select	NP_000305.3:p.Phe337Ala