Canonical Allele Identifier: CA891835843

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960997_87960998delinsCT , CM000672.2:g.87960997_87960998delinsCT	GRCh38
NC_000010.10:g.89720754_89720755delinsCT , CM000672.1:g.89720754_89720755delinsCT	GRCh37
NC_000010.9:g.89710734_89710735delinsCT	NCBI36
NG_007466.2:g.102559_102560delinsCT , LRG_311:g.102559_102560delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.998_999delinsCT	ENSP00000514759.2:p.Ser333Thr
ENST00000710265.1:c.905_906delinsCT	ENSP00000518161.1:p.Ser302Thr
ENST00000472832.3:c.905_906delinsCT	ENSP00000483066.2:p.Ser302Thr
ENST00000688158.2:n.1640_1641delinsCT
ENST00000688922.2:c.*735_*736delinsCT	ENSP00000508742.2:n.*735_*736delinsCT
ENST00000700021.1:c.860_861delinsCT	ENSP00000514757.1:p.Ser287Thr
ENST00000700022.1:c.*244_*245delinsCT	ENSP00000514758.1:n.*244_*245delinsCT
ENST00000700023.1:n.2063_2064delinsCT
ENST00000700024.1:n.2297_2298delinsCT
ENST00000700025.1:n.1674_1675delinsCT
ENST00000700026.1:n.542_543delinsCT
ENST00000706954.1:c.905_906delinsCT	ENSP00000516674.1:p.Ser302Thr
ENST00000706955.1:c.*940_*941delinsCT	ENSP00000516675.1:n.*940_*941delinsCT
ENST00000686459.1:c.*491_*492delinsCT	ENSP00000508909.1:n.*491_*492delinsCT
ENST00000688158.1:c.*1016_*1017delinsCT	ENSP00000509254.1:n.*1016_*1017delinsCT
ENST00000688308.1:c.905_906delinsCT	ENSP00000508752.1:p.Ser302Thr
ENST00000688922.1:c.826_827delinsCT
ENST00000693560.1:c.1424_1425delinsCT	ENSP00000509861.1:p.Ser475Thr
ENST00000371953.8:c.905_906delinsCT MANE Select	ENSP00000361021.3:p.Ser302Thr
ENST00000371953.7:c.905_906delinsCT	ENSP00000361021.3:p.Ser302Thr
ENST00000472832.2:c.332_333delinsCT	ENSP00000483066.1:p.Ser111Thr
NM_000314.5:c.905_906delinsCT	NP_000305.3:p.Ser302Thr
NM_000314.6:c.905_906delinsCT	NP_000305.3:p.Ser302Thr
NM_001304717.2:c.1424_1425delinsCT	NP_001291646.2:p.Ser475Thr
NM_001304718.1:c.314_315delinsCT	NP_001291647.1:p.Ser105Thr
XM_006717926.2:c.860_861delinsCT	XP_006717989.1:p.Ser287Thr
XM_011539981.1:c.905_906delinsCT	XP_011538283.1:p.Ser302Thr
XM_011539982.1:c.809_810delinsCT	XP_011538284.1:p.Ser270Thr
XR_945791.1:n.1475_1476delinsCT
NM_000314.7:c.905_906delinsCT	NP_000305.3:p.Ser302Thr
NM_001304717.5:c.1424_1425delinsCT	NP_001291646.4:p.Ser475Thr
NM_001304718.2:c.314_315delinsCT	NP_001291647.1:p.Ser105Thr
NM_000314.8:c.905_906delinsCT MANE Select	NP_000305.3:p.Ser302Thr