Canonical Allele Identifier: CA891835814

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960996_87960998delinsTAT , CM000672.2:g.87960996_87960998delinsTAT	GRCh38
NC_000010.10:g.89720753_89720755delinsTAT , CM000672.1:g.89720753_89720755delinsTAT	GRCh37
NC_000010.9:g.89710733_89710735delinsTAT	NCBI36
NG_007466.2:g.102558_102560delinsTAT , LRG_311:g.102558_102560delinsTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.997_999delinsTAT	ENSP00000514759.2:p.Ser333Tyr
ENST00000710265.1:c.904_906delinsTAT	ENSP00000518161.1:p.Ser302Tyr
ENST00000472832.3:c.904_906delinsTAT	ENSP00000483066.2:p.Ser302Tyr
ENST00000688158.2:n.1639_1641delinsTAT
ENST00000688922.2:c.*734_*736delinsTAT	ENSP00000508742.2:n.*734_*736delinsTAT
ENST00000700021.1:c.859_861delinsTAT	ENSP00000514757.1:p.Ser287Tyr
ENST00000700022.1:c.*243_*245delinsTAT	ENSP00000514758.1:n.*243_*245delinsTAT
ENST00000700023.1:n.2062_2064delinsTAT
ENST00000700024.1:n.2296_2298delinsTAT
ENST00000700025.1:n.1673_1675delinsTAT
ENST00000700026.1:n.541_543delinsTAT
ENST00000706954.1:c.904_906delinsTAT	ENSP00000516674.1:p.Ser302Tyr
ENST00000706955.1:c.*939_*941delinsTAT	ENSP00000516675.1:n.*939_*941delinsTAT
ENST00000686459.1:c.*490_*492delinsTAT	ENSP00000508909.1:n.*490_*492delinsTAT
ENST00000688158.1:c.*1015_*1017delinsTAT	ENSP00000509254.1:n.*1015_*1017delinsTAT
ENST00000688308.1:c.904_906delinsTAT	ENSP00000508752.1:p.Ser302Tyr
ENST00000688922.1:c.825_827delinsTAT
ENST00000693560.1:c.1423_1425delinsTAT	ENSP00000509861.1:p.Ser475Tyr
ENST00000371953.8:c.904_906delinsTAT MANE Select	ENSP00000361021.3:p.Ser302Tyr
ENST00000371953.7:c.904_906delinsTAT	ENSP00000361021.3:p.Ser302Tyr
ENST00000472832.2:c.331_333delinsTAT	ENSP00000483066.1:p.Ser111Tyr
NM_000314.5:c.904_906delinsTAT	NP_000305.3:p.Ser302Tyr
NM_000314.6:c.904_906delinsTAT	NP_000305.3:p.Ser302Tyr
NM_001304717.2:c.1423_1425delinsTAT	NP_001291646.2:p.Ser475Tyr
NM_001304718.1:c.313_315delinsTAT	NP_001291647.1:p.Ser105Tyr
XM_006717926.2:c.859_861delinsTAT	XP_006717989.1:p.Ser287Tyr
XM_011539981.1:c.904_906delinsTAT	XP_011538283.1:p.Ser302Tyr
XM_011539982.1:c.808_810delinsTAT	XP_011538284.1:p.Ser270Tyr
XR_945791.1:n.1474_1476delinsTAT
NM_000314.7:c.904_906delinsTAT	NP_000305.3:p.Ser302Tyr
NM_001304717.5:c.1423_1425delinsTAT	NP_001291646.4:p.Ser475Tyr
NM_001304718.2:c.313_315delinsTAT	NP_001291647.1:p.Ser105Tyr
NM_000314.8:c.904_906delinsTAT MANE Select	NP_000305.3:p.Ser302Tyr