Canonical Allele Identifier: CA891837008

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965297_87965298delinsCT , CM000672.2:g.87965297_87965298delinsCT	GRCh38
NC_000010.10:g.89725054_89725055delinsCT , CM000672.1:g.89725054_89725055delinsCT	GRCh37
NC_000010.9:g.89715034_89715035delinsCT	NCBI36
NG_007466.2:g.106859_106860delinsCT , LRG_311:g.106859_106860delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1130_1131delinsCT	ENSP00000514759.2:p.Tyr377Ser
ENST00000710265.1:c.*66_*67delinsCT	ENSP00000518161.1:n.*66_*67delinsCT
ENST00000688158.2:n.1772_1773delinsCT
ENST00000688922.2:c.*867_*868delinsCT	ENSP00000508742.2:n.*867_*868delinsCT
ENST00000700021.1:c.992_993delinsCT	ENSP00000514757.1:p.Tyr331Ser
ENST00000700022.1:c.*376_*377delinsCT	ENSP00000514758.1:n.*376_*377delinsCT
ENST00000700023.1:n.2195_2196delinsCT
ENST00000700024.1:n.2429_2430delinsCT
ENST00000706954.1:c.1037_1038delinsCT	ENSP00000516674.1:p.Tyr346Ser
ENST00000706955.1:c.*1072_*1073delinsCT	ENSP00000516675.1:n.*1072_*1073delinsCT
ENST00000686459.1:c.*623_*624delinsCT	ENSP00000508909.1:n.*623_*624delinsCT
ENST00000688158.1:c.*1148_*1149delinsCT	ENSP00000509254.1:n.*1148_*1149delinsCT
ENST00000688308.1:c.1037_1038delinsCT	ENSP00000508752.1:p.Tyr346Ser
ENST00000688922.1:c.958_959delinsCT
ENST00000693560.1:c.1556_1557delinsCT	ENSP00000509861.1:p.Tyr519Ser
ENST00000371953.8:c.1037_1038delinsCT MANE Select	ENSP00000361021.3:p.Tyr346Ser
ENST00000371953.7:c.1037_1038delinsCT	ENSP00000361021.3:p.Tyr346Ser
NM_000314.5:c.1037_1038delinsCT	NP_000305.3:p.Tyr346Ser
NM_000314.6:c.1037_1038delinsCT	NP_000305.3:p.Tyr346Ser
NM_001304717.2:c.1556_1557delinsCT	NP_001291646.2:p.Tyr519Ser
NM_001304718.1:c.446_447delinsCT	NP_001291647.1:p.Tyr149Ser
XM_006717926.2:c.992_993delinsCT	XP_006717989.1:p.Tyr331Ser
XM_011539982.1:c.941_942delinsCT	XP_011538284.1:p.Tyr314Ser
XR_945791.1:n.1607_1608delinsCT
NM_000314.7:c.1037_1038delinsCT	NP_000305.3:p.Tyr346Ser
NM_001304717.5:c.1556_1557delinsCT	NP_001291646.4:p.Tyr519Ser
NM_001304718.2:c.446_447delinsCT	NP_001291647.1:p.Tyr149Ser
NM_000314.8:c.1037_1038delinsCT MANE Select	NP_000305.3:p.Tyr346Ser