Canonical Allele Identifier: CA891841422

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961101_87961102delinsGG , CM000672.2:g.87961101_87961102delinsGG	GRCh38
NC_000010.10:g.89720858_89720859delinsGG , CM000672.1:g.89720858_89720859delinsGG	GRCh37
NC_000010.9:g.89710838_89710839delinsGG	NCBI36
NG_007466.2:g.102663_102664delinsGG , LRG_311:g.102663_102664delinsGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1102_1103delinsGG	ENSP00000514759.2:p.Phe368Gly
ENST00000710265.1:c.1009_1010delinsGG	ENSP00000518161.1:p.Phe337Gly
ENST00000472832.3:c.1009_1010delinsGG	ENSP00000483066.2:p.Phe337Gly
ENST00000688158.2:n.1744_1745delinsGG
ENST00000688922.2:c.*839_*840delinsGG	ENSP00000508742.2:n.*839_*840delinsGG
ENST00000700021.1:c.964_965delinsGG	ENSP00000514757.1:p.Phe322Gly
ENST00000700022.1:c.*348_*349delinsGG	ENSP00000514758.1:n.*348_*349delinsGG
ENST00000700023.1:n.2167_2168delinsGG
ENST00000700024.1:n.2401_2402delinsGG
ENST00000700025.1:n.1778_1779delinsGG
ENST00000700026.1:n.646_647delinsGG
ENST00000706954.1:c.1009_1010delinsGG	ENSP00000516674.1:p.Phe337Gly
ENST00000706955.1:c.*1044_*1045delinsGG	ENSP00000516675.1:n.*1044_*1045delinsGG
ENST00000686459.1:c.*595_*596delinsGG	ENSP00000508909.1:n.*595_*596delinsGG
ENST00000688158.1:c.*1120_*1121delinsGG	ENSP00000509254.1:n.*1120_*1121delinsGG
ENST00000688308.1:c.1009_1010delinsGG	ENSP00000508752.1:p.Phe337Gly
ENST00000688922.1:c.930_931delinsGG
ENST00000693560.1:c.1528_1529delinsGG	ENSP00000509861.1:p.Phe510Gly
ENST00000371953.8:c.1009_1010delinsGG MANE Select	ENSP00000361021.3:p.Phe337Gly
ENST00000371953.7:c.1009_1010delinsGG	ENSP00000361021.3:p.Phe337Gly
ENST00000472832.2:c.436_437delinsGG	ENSP00000483066.1:p.Phe146Gly
NM_000314.5:c.1009_1010delinsGG	NP_000305.3:p.Phe337Gly
NM_000314.6:c.1009_1010delinsGG	NP_000305.3:p.Phe337Gly
NM_001304717.2:c.1528_1529delinsGG	NP_001291646.2:p.Phe510Gly
NM_001304718.1:c.418_419delinsGG	NP_001291647.1:p.Phe140Gly
XM_006717926.2:c.964_965delinsGG	XP_006717989.1:p.Phe322Gly
XM_011539981.1:c.1009_1010delinsGG	XP_011538283.1:p.Phe337Gly
XM_011539982.1:c.913_914delinsGG	XP_011538284.1:p.Phe305Gly
XR_945791.1:n.1579_1580delinsGG
NM_000314.7:c.1009_1010delinsGG	NP_000305.3:p.Phe337Gly
NM_001304717.5:c.1528_1529delinsGG	NP_001291646.4:p.Phe510Gly
NM_001304718.2:c.418_419delinsGG	NP_001291647.1:p.Phe140Gly
NM_000314.8:c.1009_1010delinsGG MANE Select	NP_000305.3:p.Phe337Gly