Canonical Allele Identifier: CA891836656

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961057_87961058delinsCT , CM000672.2:g.87961057_87961058delinsCT	GRCh38
NC_000010.10:g.89720814_89720815delinsCT , CM000672.1:g.89720814_89720815delinsCT	GRCh37
NC_000010.9:g.89710794_89710795delinsCT	NCBI36
NG_007466.2:g.102619_102620delinsCT , LRG_311:g.102619_102620delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1058_1059delinsCT	ENSP00000514759.2:p.Lys353Thr
ENST00000710265.1:c.965_966delinsCT	ENSP00000518161.1:p.Lys322Thr
ENST00000472832.3:c.965_966delinsCT	ENSP00000483066.2:p.Lys322Thr
ENST00000688158.2:n.1700_1701delinsCT
ENST00000688922.2:c.*795_*796delinsCT	ENSP00000508742.2:n.*795_*796delinsCT
ENST00000700021.1:c.920_921delinsCT	ENSP00000514757.1:p.Lys307Thr
ENST00000700022.1:c.*304_*305delinsCT	ENSP00000514758.1:n.*304_*305delinsCT
ENST00000700023.1:n.2123_2124delinsCT
ENST00000700024.1:n.2357_2358delinsCT
ENST00000700025.1:n.1734_1735delinsCT
ENST00000700026.1:n.602_603delinsCT
ENST00000706954.1:c.965_966delinsCT	ENSP00000516674.1:p.Lys322Thr
ENST00000706955.1:c.*1000_*1001delinsCT	ENSP00000516675.1:n.*1000_*1001delinsCT
ENST00000686459.1:c.*551_*552delinsCT	ENSP00000508909.1:n.*551_*552delinsCT
ENST00000688158.1:c.*1076_*1077delinsCT	ENSP00000509254.1:n.*1076_*1077delinsCT
ENST00000688308.1:c.965_966delinsCT	ENSP00000508752.1:p.Lys322Thr
ENST00000688922.1:c.886_887delinsCT
ENST00000693560.1:c.1484_1485delinsCT	ENSP00000509861.1:p.Lys495Thr
ENST00000371953.8:c.965_966delinsCT MANE Select	ENSP00000361021.3:p.Lys322Thr
ENST00000371953.7:c.965_966delinsCT	ENSP00000361021.3:p.Lys322Thr
ENST00000472832.2:c.392_393delinsCT	ENSP00000483066.1:p.Lys131Thr
NM_000314.5:c.965_966delinsCT	NP_000305.3:p.Lys322Thr
NM_000314.6:c.965_966delinsCT	NP_000305.3:p.Lys322Thr
NM_001304717.2:c.1484_1485delinsCT	NP_001291646.2:p.Lys495Thr
NM_001304718.1:c.374_375delinsCT	NP_001291647.1:p.Lys125Thr
XM_006717926.2:c.920_921delinsCT	XP_006717989.1:p.Lys307Thr
XM_011539981.1:c.965_966delinsCT	XP_011538283.1:p.Lys322Thr
XM_011539982.1:c.869_870delinsCT	XP_011538284.1:p.Lys290Thr
XR_945791.1:n.1535_1536delinsCT
NM_000314.7:c.965_966delinsCT	NP_000305.3:p.Lys322Thr
NM_001304717.5:c.1484_1485delinsCT	NP_001291646.4:p.Lys495Thr
NM_001304718.2:c.374_375delinsCT	NP_001291647.1:p.Lys125Thr
NM_000314.8:c.965_966delinsCT MANE Select	NP_000305.3:p.Lys322Thr