Canonical Allele Identifier: CA891841326

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961080_87961081delinsGT , CM000672.2:g.87961080_87961081delinsGT	GRCh38
NC_000010.10:g.89720837_89720838delinsGT , CM000672.1:g.89720837_89720838delinsGT	GRCh37
NC_000010.9:g.89710817_89710818delinsGT	NCBI36
NG_007466.2:g.102642_102643delinsGT , LRG_311:g.102642_102643delinsGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.1081_1082delinsGT	ENSP00000514759.2:p.Lys361Val
ENST00000710265.1:c.988_989delinsGT	ENSP00000518161.1:p.Lys330Val
ENST00000472832.3:c.988_989delinsGT	ENSP00000483066.2:p.Lys330Val
ENST00000688158.2:n.1723_1724delinsGT
ENST00000688922.2:c.*818_*819delinsGT	ENSP00000508742.2:n.*818_*819delinsGT
ENST00000700021.1:c.943_944delinsGT	ENSP00000514757.1:p.Lys315Val
ENST00000700022.1:c.*327_*328delinsGT	ENSP00000514758.1:n.*327_*328delinsGT
ENST00000700023.1:n.2146_2147delinsGT
ENST00000700024.1:n.2380_2381delinsGT
ENST00000700025.1:n.1757_1758delinsGT
ENST00000700026.1:n.625_626delinsGT
ENST00000706954.1:c.988_989delinsGT	ENSP00000516674.1:p.Lys330Val
ENST00000706955.1:c.*1023_*1024delinsGT	ENSP00000516675.1:n.*1023_*1024delinsGT
ENST00000686459.1:c.*574_*575delinsGT	ENSP00000508909.1:n.*574_*575delinsGT
ENST00000688158.1:c.*1099_*1100delinsGT	ENSP00000509254.1:n.*1099_*1100delinsGT
ENST00000688308.1:c.988_989delinsGT	ENSP00000508752.1:p.Lys330Val
ENST00000688922.1:c.909_910delinsGT
ENST00000693560.1:c.1507_1508delinsGT	ENSP00000509861.1:p.Lys503Val
ENST00000371953.8:c.988_989delinsGT MANE Select	ENSP00000361021.3:p.Lys330Val
ENST00000371953.7:c.988_989delinsGT	ENSP00000361021.3:p.Lys330Val
ENST00000472832.2:c.415_416delinsGT	ENSP00000483066.1:p.Lys139Val
NM_000314.5:c.988_989delinsGT	NP_000305.3:p.Lys330Val
NM_000314.6:c.988_989delinsGT	NP_000305.3:p.Lys330Val
NM_001304717.2:c.1507_1508delinsGT	NP_001291646.2:p.Lys503Val
NM_001304718.1:c.397_398delinsGT	NP_001291647.1:p.Lys133Val
XM_006717926.2:c.943_944delinsGT	XP_006717989.1:p.Lys315Val
XM_011539981.1:c.988_989delinsGT	XP_011538283.1:p.Lys330Val
XM_011539982.1:c.892_893delinsGT	XP_011538284.1:p.Lys298Val
XR_945791.1:n.1558_1559delinsGT
NM_000314.7:c.988_989delinsGT	NP_000305.3:p.Lys330Val
NM_001304717.5:c.1507_1508delinsGT	NP_001291646.4:p.Lys503Val
NM_001304718.2:c.397_398delinsGT	NP_001291647.1:p.Lys133Val
NM_000314.8:c.988_989delinsGT MANE Select	NP_000305.3:p.Lys330Val