Canonical Allele Identifier: CA891837173

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965323_87965324delinsGA , CM000672.2:g.87965323_87965324delinsGA	GRCh38
NC_000010.10:g.89725080_89725081delinsGA , CM000672.1:g.89725080_89725081delinsGA	GRCh37
NC_000010.9:g.89715060_89715061delinsGA	NCBI36
NG_007466.2:g.106885_106886delinsGA , LRG_311:g.106885_106886delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1156_1157delinsGA	ENSP00000514759.2:p.Ser386Glu
ENST00000710265.1:c.*92_*93delinsGA	ENSP00000518161.1:n.*92_*93delinsGA
ENST00000688158.2:n.1798_1799delinsGA
ENST00000688922.2:c.*893_*894delinsGA	ENSP00000508742.2:n.*893_*894delinsGA
ENST00000700021.1:c.1018_1019delinsGA	ENSP00000514757.1:p.Ser340Glu
ENST00000700022.1:c.*402_*403delinsGA	ENSP00000514758.1:n.*402_*403delinsGA
ENST00000700023.1:n.2221_2222delinsGA
ENST00000700024.1:n.2455_2456delinsGA
ENST00000706954.1:c.1063_1064delinsGA	ENSP00000516674.1:p.Ser355Glu
ENST00000706955.1:c.*1098_*1099delinsGA	ENSP00000516675.1:n.*1098_*1099delinsGA
ENST00000686459.1:c.*649_*650delinsGA	ENSP00000508909.1:n.*649_*650delinsGA
ENST00000688158.1:c.*1174_*1175delinsGA	ENSP00000509254.1:n.*1174_*1175delinsGA
ENST00000688308.1:c.1063_1064delinsGA	ENSP00000508752.1:p.Ser355Glu
ENST00000688922.1:c.984_985delinsGA
ENST00000693560.1:c.1582_1583delinsGA	ENSP00000509861.1:p.Ser528Glu
ENST00000371953.8:c.1063_1064delinsGA MANE Select	ENSP00000361021.3:p.Ser355Glu
ENST00000371953.7:c.1063_1064delinsGA	ENSP00000361021.3:p.Ser355Glu
NM_000314.5:c.1063_1064delinsGA	NP_000305.3:p.Ser355Glu
NM_000314.6:c.1063_1064delinsGA	NP_000305.3:p.Ser355Glu
NM_001304717.2:c.1582_1583delinsGA	NP_001291646.2:p.Ser528Glu
NM_001304718.1:c.472_473delinsGA	NP_001291647.1:p.Ser158Glu
XM_006717926.2:c.1018_1019delinsGA	XP_006717989.1:p.Ser340Glu
XM_011539982.1:c.967_968delinsGA	XP_011538284.1:p.Ser323Glu
XR_945791.1:n.1633_1634delinsGA
NM_000314.7:c.1063_1064delinsGA	NP_000305.3:p.Ser355Glu
NM_001304717.5:c.1582_1583delinsGA	NP_001291646.4:p.Ser528Glu
NM_001304718.2:c.472_473delinsGA	NP_001291647.1:p.Ser158Glu
NM_000314.8:c.1063_1064delinsGA MANE Select	NP_000305.3:p.Ser355Glu