Canonical Allele Identifier: CA891841493

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965290_87965292delinsGAT , CM000672.2:g.87965290_87965292delinsGAT	GRCh38
NC_000010.10:g.89725047_89725049delinsGAT , CM000672.1:g.89725047_89725049delinsGAT	GRCh37
NC_000010.9:g.89715027_89715029delinsGAT	NCBI36
NG_007466.2:g.106852_106854delinsGAT , LRG_311:g.106852_106854delinsGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1123_1125delinsGAT	ENSP00000514759.2:p.Lys375Asp
ENST00000710265.1:c.*59_*61delinsGAT	ENSP00000518161.1:n.*59_*61delinsGAT
ENST00000688158.2:n.1765_1767delinsGAT
ENST00000688922.2:c.*860_*862delinsGAT	ENSP00000508742.2:n.*860_*862delinsGAT
ENST00000700021.1:c.985_987delinsGAT	ENSP00000514757.1:p.Lys329Asp
ENST00000700022.1:c.*369_*371delinsGAT	ENSP00000514758.1:n.*369_*371delinsGAT
ENST00000700023.1:n.2188_2190delinsGAT
ENST00000700024.1:n.2422_2424delinsGAT
ENST00000706954.1:c.1030_1032delinsGAT	ENSP00000516674.1:p.Lys344Asp
ENST00000706955.1:c.*1065_*1067delinsGAT	ENSP00000516675.1:n.*1065_*1067delinsGAT
ENST00000686459.1:c.*616_*618delinsGAT	ENSP00000508909.1:n.*616_*618delinsGAT
ENST00000688158.1:c.*1141_*1143delinsGAT	ENSP00000509254.1:n.*1141_*1143delinsGAT
ENST00000688308.1:c.1030_1032delinsGAT	ENSP00000508752.1:p.Lys344Asp
ENST00000688922.1:c.951_953delinsGAT
ENST00000693560.1:c.1549_1551delinsGAT	ENSP00000509861.1:p.Lys517Asp
ENST00000371953.8:c.1030_1032delinsGAT MANE Select	ENSP00000361021.3:p.Lys344Asp
ENST00000371953.7:c.1030_1032delinsGAT	ENSP00000361021.3:p.Lys344Asp
NM_000314.5:c.1030_1032delinsGAT	NP_000305.3:p.Lys344Asp
NM_000314.6:c.1030_1032delinsGAT	NP_000305.3:p.Lys344Asp
NM_001304717.2:c.1549_1551delinsGAT	NP_001291646.2:p.Lys517Asp
NM_001304718.1:c.439_441delinsGAT	NP_001291647.1:p.Lys147Asp
XM_006717926.2:c.985_987delinsGAT	XP_006717989.1:p.Lys329Asp
XM_011539982.1:c.934_936delinsGAT	XP_011538284.1:p.Lys312Asp
XR_945791.1:n.1600_1602delinsGAT
NM_000314.7:c.1030_1032delinsGAT	NP_000305.3:p.Lys344Asp
NM_001304717.5:c.1549_1551delinsGAT	NP_001291646.4:p.Lys517Asp
NM_001304718.2:c.439_441delinsGAT	NP_001291647.1:p.Lys147Asp
NM_000314.8:c.1030_1032delinsGAT MANE Select	NP_000305.3:p.Lys344Asp