Canonical Allele Identifier: CA1926176330

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87933248_87933253delinsAAAGGT , CM000672.2:g.87933248_87933253delinsAAAGGT	GRCh38
NC_000010.10:g.89693005_89693010delinsAAAGGT , CM000672.1:g.89693005_89693010delinsAAAGGT	GRCh37
NC_000010.9:g.89682985_89682990delinsAAAGGT	NCBI36
NG_007466.2:g.74810_74815delinsAAAGGT , LRG_311:g.74810_74815delinsAAAGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.489_492+2delinsAAAGGT
ENST00000710265.1:c.489_492+2delinsAAAGGT
ENST00000472832.3:c.489_492+2delinsAAAGGT
ENST00000688158.2:n.1224_1227+2delinsAAAGGT
ENST00000688922.2:c.*319_*322+2delinsAAAGGT
ENST00000700021.1:c.444_447+2delinsAAAGGT
ENST00000700022.1:c.489_492+2delinsAAAGGT
ENST00000700029.1:c.323_326+2delinsAAAGGT
ENST00000706954.1:c.489_492+2delinsAAAGGT
ENST00000706955.1:c.*524_*527+2delinsAAAGGT
ENST00000686459.1:c.489_492+2delinsAAAGGT
ENST00000688158.1:c.*600_*603+2delinsAAAGGT
ENST00000688308.1:c.489_492+2delinsAAAGGT
ENST00000688922.1:c.410_413+2delinsAAAGGT
ENST00000693560.1:c.1008_1011+2delinsAAAGGT
ENST00000371953.8:c.489_492+2delinsAAAGGT
ENST00000371953.7:c.489_492+2delinsAAAGGT
ENST00000498703.1:n.315_320delinsAAAGGT
ENST00000610634.1:c.387_390+2delinsAAAGGT
NM_000314.5:c.489_492+2delinsAAAGGT
NM_000314.6:c.489_492+2delinsAAAGGT
NM_001304717.2:c.1008_1011+2delinsAAAGGT
NM_001304718.1:c.-262_-259+2delinsAAAGGT
XM_006717926.2:c.444_447+2delinsAAAGGT
XM_011539981.1:c.489_492+2delinsAAAGGT
XM_011539982.1:c.393_396+2delinsAAAGGT
XR_945789.1:n.1201_1204+2delinsAAAGGT
XR_945790.1:n.1201_1204+2delinsAAAGGT
XR_945791.1:n.1201_1204+2delinsAAAGGT
NM_000314.7:c.489_492+2delinsAAAGGT
NM_001304717.5:c.1008_1011+2delinsAAAGGT
NM_001304718.2:c.-262_-259+2delinsAAAGGT
NM_000314.8:c.489_492+2delinsAAAGGT