Canonical Allele Identifier: CA891836379

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961032_87961034delinsTAT , CM000672.2:g.87961032_87961034delinsTAT	GRCh38
NC_000010.10:g.89720789_89720791delinsTAT , CM000672.1:g.89720789_89720791delinsTAT	GRCh37
NC_000010.9:g.89710769_89710771delinsTAT	NCBI36
NG_007466.2:g.102594_102596delinsTAT , LRG_311:g.102594_102596delinsTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1033_1035delinsTAT	ENSP00000514759.2:p.Glu345Tyr
ENST00000710265.1:c.940_942delinsTAT	ENSP00000518161.1:p.Glu314Tyr
ENST00000472832.3:c.940_942delinsTAT	ENSP00000483066.2:p.Glu314Tyr
ENST00000688158.2:n.1675_1677delinsTAT
ENST00000688922.2:c.*770_*772delinsTAT	ENSP00000508742.2:n.*770_*772delinsTAT
ENST00000700021.1:c.895_897delinsTAT	ENSP00000514757.1:p.Glu299Tyr
ENST00000700022.1:c.*279_*281delinsTAT	ENSP00000514758.1:n.*279_*281delinsTAT
ENST00000700023.1:n.2098_2100delinsTAT
ENST00000700024.1:n.2332_2334delinsTAT
ENST00000700025.1:n.1709_1711delinsTAT
ENST00000700026.1:n.577_579delinsTAT
ENST00000706954.1:c.940_942delinsTAT	ENSP00000516674.1:p.Glu314Tyr
ENST00000706955.1:c.*975_*977delinsTAT	ENSP00000516675.1:n.*975_*977delinsTAT
ENST00000686459.1:c.*526_*528delinsTAT	ENSP00000508909.1:n.*526_*528delinsTAT
ENST00000688158.1:c.*1051_*1053delinsTAT	ENSP00000509254.1:n.*1051_*1053delinsTAT
ENST00000688308.1:c.940_942delinsTAT	ENSP00000508752.1:p.Glu314Tyr
ENST00000688922.1:c.861_863delinsTAT
ENST00000693560.1:c.1459_1461delinsTAT	ENSP00000509861.1:p.Glu487Tyr
ENST00000371953.8:c.940_942delinsTAT MANE Select	ENSP00000361021.3:p.Glu314Tyr
ENST00000371953.7:c.940_942delinsTAT	ENSP00000361021.3:p.Glu314Tyr
ENST00000472832.2:c.367_369delinsTAT	ENSP00000483066.1:p.Glu123Tyr
NM_000314.5:c.940_942delinsTAT	NP_000305.3:p.Glu314Tyr
NM_000314.6:c.940_942delinsTAT	NP_000305.3:p.Glu314Tyr
NM_001304717.2:c.1459_1461delinsTAT	NP_001291646.2:p.Glu487Tyr
NM_001304718.1:c.349_351delinsTAT	NP_001291647.1:p.Glu117Tyr
XM_006717926.2:c.895_897delinsTAT	XP_006717989.1:p.Glu299Tyr
XM_011539981.1:c.940_942delinsTAT	XP_011538283.1:p.Glu314Tyr
XM_011539982.1:c.844_846delinsTAT	XP_011538284.1:p.Glu282Tyr
XR_945791.1:n.1510_1512delinsTAT
NM_000314.7:c.940_942delinsTAT	NP_000305.3:p.Glu314Tyr
NM_001304717.5:c.1459_1461delinsTAT	NP_001291646.4:p.Glu487Tyr
NM_001304718.2:c.349_351delinsTAT	NP_001291647.1:p.Glu117Tyr
NM_000314.8:c.940_942delinsTAT MANE Select	NP_000305.3:p.Glu314Tyr