Canonical Allele Identifier: CA2579927103

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87894076_87894078del , CM000672.2:g.87894076_87894078del	GRCh38
NC_000010.10:g.89653833_89653835del , CM000672.1:g.89653833_89653835del	GRCh37
NC_000010.9:g.89643813_89643815del	NCBI36
NG_007466.2:g.35638_35640del , LRG_311:g.35638_35640del

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.131_133del	ENSP00000514759.2:p.Gly44del
ENST00000710265.1:c.131_133del	ENSP00000518161.1:p.Gly44del
ENST00000472832.3:c.131_133del	ENSP00000483066.2:p.Gly44del
ENST00000688158.2:n.899+13638_899+13640del
ENST00000688922.2:c.131_133del	ENSP00000508742.2:p.Gly44del
ENST00000700021.1:c.131_133del	ENSP00000514757.1:p.Gly44del
ENST00000700022.1:c.131_133del	ENSP00000514758.1:p.Gly44del
ENST00000706954.1:c.131_133del	ENSP00000516674.1:p.Gly44del
ENST00000706955.1:c.*166_*168del	ENSP00000516675.1:n.*166_*168del
ENST00000686459.1:c.131_133del	ENSP00000508909.1:p.Gly44del
ENST00000688158.1:c.*275+13638_*275+13640del	ENSP00000509254.1:n.*275+13638_*275+13640del
ENST00000688308.1:c.131_133del	ENSP00000508752.1:p.Gly44del
ENST00000693560.1:c.650_652del	ENSP00000509861.1:p.Gly217del
ENST00000371953.8:c.131_133del MANE Select	ENSP00000361021.3:p.Gly44del
ENST00000371953.7:c.131_133del	ENSP00000361021.3:p.Gly44del
ENST00000462694.1:n.133_135del
ENST00000610634.1:c.29_31del	ENSP00000477517.1:p.Gly10del
NM_000314.5:c.131_133del	NP_000305.3:p.Gly44del
NM_000314.6:c.131_133del	NP_000305.3:p.Gly44del
NM_001304717.2:c.650_652del	NP_001291646.2:p.Gly217del
NM_001304718.1:c.-575_-573del	NP_001291647.1:n.-575_-573del
XM_006717926.2:c.131_133del	XP_006717989.1:p.Gly44del
XM_011539981.1:c.131_133del	XP_011538283.1:p.Gly44del
XM_011539982.1:c.68+13638_68+13640del	XP_011538284.1:n.68+13638_68+13640del
XR_945789.1:n.843_845del
XR_945790.1:n.843_845del
XR_945791.1:n.843_845del
NM_000314.7:c.131_133del	NP_000305.3:p.Gly44del
NM_001304717.5:c.650_652del	NP_001291646.4:p.Gly217del
NM_001304718.2:c.-575_-573del	NP_001291647.1:n.-575_-573del
NM_000314.8:c.131_133del MANE Select	NP_000305.3:p.Gly44del