Canonical Allele Identifier: CA891835134

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87894075_87894077delinsTGT , CM000672.2:g.87894075_87894077delinsTGT	GRCh38
NC_000010.10:g.89653832_89653834delinsTGT , CM000672.1:g.89653832_89653834delinsTGT	GRCh37
NC_000010.9:g.89643812_89643814delinsTGT	NCBI36
NG_007466.2:g.35637_35639delinsTGT , LRG_311:g.35637_35639delinsTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.130_132delinsTGT	ENSP00000514759.2:p.Gly44Cys
ENST00000710265.1:c.130_132delinsTGT	ENSP00000518161.1:p.Gly44Cys
ENST00000472832.3:c.130_132delinsTGT	ENSP00000483066.2:p.Gly44Cys
ENST00000688158.2:n.899+13637_899+13639delinsTGT
ENST00000688922.2:c.130_132delinsTGT	ENSP00000508742.2:p.Gly44Cys
ENST00000700021.1:c.130_132delinsTGT	ENSP00000514757.1:p.Gly44Cys
ENST00000700022.1:c.130_132delinsTGT	ENSP00000514758.1:p.Gly44Cys
ENST00000706954.1:c.130_132delinsTGT	ENSP00000516674.1:p.Gly44Cys
ENST00000706955.1:c.*165_*167delinsTGT	ENSP00000516675.1:n.*165_*167delinsTGT
ENST00000686459.1:c.130_132delinsTGT	ENSP00000508909.1:p.Gly44Cys
ENST00000688158.1:c.*275+13637_*275+13639delinsTGT	ENSP00000509254.1:n.*275+13637_*275+13639delinsTGT
ENST00000688308.1:c.130_132delinsTGT	ENSP00000508752.1:p.Gly44Cys
ENST00000693560.1:c.649_651delinsTGT	ENSP00000509861.1:p.Gly217Cys
ENST00000371953.8:c.130_132delinsTGT MANE Select	ENSP00000361021.3:p.Gly44Cys
ENST00000371953.7:c.130_132delinsTGT	ENSP00000361021.3:p.Gly44Cys
ENST00000462694.1:n.132_134delinsTGT
ENST00000610634.1:c.28_30delinsTGT	ENSP00000477517.1:p.Gly10Cys
NM_000314.5:c.130_132delinsTGT	NP_000305.3:p.Gly44Cys
NM_000314.6:c.130_132delinsTGT	NP_000305.3:p.Gly44Cys
NM_001304717.2:c.649_651delinsTGT	NP_001291646.2:p.Gly217Cys
NM_001304718.1:c.-576_-574delinsTGT	NP_001291647.1:n.-576_-574delinsTGT
XM_006717926.2:c.130_132delinsTGT	XP_006717989.1:p.Gly44Cys
XM_011539981.1:c.130_132delinsTGT	XP_011538283.1:p.Gly44Cys
XM_011539982.1:c.68+13637_68+13639delinsTGT	XP_011538284.1:n.68+13637_68+13639delinsTGT
XR_945789.1:n.842_844delinsTGT
XR_945790.1:n.842_844delinsTGT
XR_945791.1:n.842_844delinsTGT
NM_000314.7:c.130_132delinsTGT	NP_000305.3:p.Gly44Cys
NM_001304717.5:c.649_651delinsTGT	NP_001291646.4:p.Gly217Cys
NM_001304718.2:c.-576_-574delinsTGT	NP_001291647.1:n.-576_-574delinsTGT
NM_000314.8:c.130_132delinsTGT MANE Select	NP_000305.3:p.Gly44Cys