Canonical Allele Identifier: CA891836652

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961056_87961058delinsTAT , CM000672.2:g.87961056_87961058delinsTAT	GRCh38
NC_000010.10:g.89720813_89720815delinsTAT , CM000672.1:g.89720813_89720815delinsTAT	GRCh37
NC_000010.9:g.89710793_89710795delinsTAT	NCBI36
NG_007466.2:g.102618_102620delinsTAT , LRG_311:g.102618_102620delinsTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1057_1059delinsTAT	ENSP00000514759.2:p.Lys353Tyr
ENST00000710265.1:c.964_966delinsTAT	ENSP00000518161.1:p.Lys322Tyr
ENST00000472832.3:c.964_966delinsTAT	ENSP00000483066.2:p.Lys322Tyr
ENST00000688158.2:n.1699_1701delinsTAT
ENST00000688922.2:c.*794_*796delinsTAT	ENSP00000508742.2:n.*794_*796delinsTAT
ENST00000700021.1:c.919_921delinsTAT	ENSP00000514757.1:p.Lys307Tyr
ENST00000700022.1:c.*303_*305delinsTAT	ENSP00000514758.1:n.*303_*305delinsTAT
ENST00000700023.1:n.2122_2124delinsTAT
ENST00000700024.1:n.2356_2358delinsTAT
ENST00000700025.1:n.1733_1735delinsTAT
ENST00000700026.1:n.601_603delinsTAT
ENST00000706954.1:c.964_966delinsTAT	ENSP00000516674.1:p.Lys322Tyr
ENST00000706955.1:c.*999_*1001delinsTAT	ENSP00000516675.1:n.*999_*1001delinsTAT
ENST00000686459.1:c.*550_*552delinsTAT	ENSP00000508909.1:n.*550_*552delinsTAT
ENST00000688158.1:c.*1075_*1077delinsTAT	ENSP00000509254.1:n.*1075_*1077delinsTAT
ENST00000688308.1:c.964_966delinsTAT	ENSP00000508752.1:p.Lys322Tyr
ENST00000688922.1:c.885_887delinsTAT
ENST00000693560.1:c.1483_1485delinsTAT	ENSP00000509861.1:p.Lys495Tyr
ENST00000371953.8:c.964_966delinsTAT MANE Select	ENSP00000361021.3:p.Lys322Tyr
ENST00000371953.7:c.964_966delinsTAT	ENSP00000361021.3:p.Lys322Tyr
ENST00000472832.2:c.391_393delinsTAT	ENSP00000483066.1:p.Lys131Tyr
NM_000314.5:c.964_966delinsTAT	NP_000305.3:p.Lys322Tyr
NM_000314.6:c.964_966delinsTAT	NP_000305.3:p.Lys322Tyr
NM_001304717.2:c.1483_1485delinsTAT	NP_001291646.2:p.Lys495Tyr
NM_001304718.1:c.373_375delinsTAT	NP_001291647.1:p.Lys125Tyr
XM_006717926.2:c.919_921delinsTAT	XP_006717989.1:p.Lys307Tyr
XM_011539981.1:c.964_966delinsTAT	XP_011538283.1:p.Lys322Tyr
XM_011539982.1:c.868_870delinsTAT	XP_011538284.1:p.Lys290Tyr
XR_945791.1:n.1534_1536delinsTAT
NM_000314.7:c.964_966delinsTAT	NP_000305.3:p.Lys322Tyr
NM_001304717.5:c.1483_1485delinsTAT	NP_001291646.4:p.Lys495Tyr
NM_001304718.2:c.373_375delinsTAT	NP_001291647.1:p.Lys125Tyr
NM_000314.8:c.964_966delinsTAT MANE Select	NP_000305.3:p.Lys322Tyr