Canonical Allele Identifier: CA2579926537

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965287_87965289del , CM000672.2:g.87965287_87965289del	GRCh38
NC_000010.10:g.89725044_89725046del , CM000672.1:g.89725044_89725046del	GRCh37
NC_000010.9:g.89715024_89715026del	NCBI36
NG_007466.2:g.106849_106851del , LRG_311:g.106849_106851del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1120_1122del
ENST00000710265.1:c.*56_*58del
ENST00000688158.2:n.1762_1764del
ENST00000688922.2:c.*857_*859del
ENST00000700021.1:c.982_984del
ENST00000700022.1:c.*366_*368del
ENST00000700023.1:n.2185_2187del
ENST00000700024.1:n.2419_2421del
ENST00000706954.1:c.1027_1029del
ENST00000706955.1:c.*1062_*1064del
ENST00000686459.1:c.*613_*615del
ENST00000688158.1:c.*1138_*1140del
ENST00000688308.1:c.1027_1029del
ENST00000688922.1:c.948_950del
ENST00000693560.1:c.1546_1548del
ENST00000371953.8:c.1027_1029del
ENST00000371953.7:c.1027_1029del
NM_000314.5:c.1027_1029del
NM_000314.6:c.1027_1029del
NM_001304717.2:c.1546_1548del
NM_001304718.1:c.436_438del
XM_006717926.2:c.982_984del
XM_011539982.1:c.931_933del
XR_945791.1:n.1597_1599del
NM_000314.7:c.1027_1029del
NM_001304717.5:c.1546_1548del
NM_001304718.2:c.436_438del
NM_000314.8:c.1027_1029del