Canonical Allele Identifier: CA891840916

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957996_87957997delinsGC , CM000672.2:g.87957996_87957997delinsGC	GRCh38
NC_000010.10:g.89717753_89717754delinsGC , CM000672.1:g.89717753_89717754delinsGC	GRCh37
NC_000010.9:g.89707733_89707734delinsGC	NCBI36
NG_007466.2:g.99558_99559delinsGC , LRG_311:g.99558_99559delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.778_779delinsGC	ENSP00000514759.2:p.Lys260Ala
ENST00000710265.1:c.778_779delinsGC	ENSP00000518161.1:p.Lys260Ala
ENST00000472832.3:c.778_779delinsGC	ENSP00000483066.2:p.Lys260Ala
ENST00000688158.2:n.1513_1514delinsGC
ENST00000688922.2:c.*608_*609delinsGC	ENSP00000508742.2:n.*608_*609delinsGC
ENST00000700021.1:c.733_734delinsGC	ENSP00000514757.1:p.Lys245Ala
ENST00000700022.1:c.*117_*118delinsGC	ENSP00000514758.1:n.*117_*118delinsGC
ENST00000700023.1:n.1936_1937delinsGC
ENST00000700024.1:n.2170_2171delinsGC
ENST00000700025.1:n.1547_1548delinsGC
ENST00000700026.1:n.415_416delinsGC
ENST00000700029.1:c.612_613delinsGC
ENST00000706954.1:c.778_779delinsGC	ENSP00000516674.1:p.Lys260Ala
ENST00000706955.1:c.*813_*814delinsGC	ENSP00000516675.1:n.*813_*814delinsGC
ENST00000686459.1:c.*364_*365delinsGC	ENSP00000508909.1:n.*364_*365delinsGC
ENST00000688158.1:c.*889_*890delinsGC	ENSP00000509254.1:n.*889_*890delinsGC
ENST00000688308.1:c.778_779delinsGC	ENSP00000508752.1:p.Lys260Ala
ENST00000688922.1:c.699_700delinsGC
ENST00000693560.1:c.1297_1298delinsGC	ENSP00000509861.1:p.Lys433Ala
ENST00000371953.8:c.778_779delinsGC MANE Select	ENSP00000361021.3:p.Lys260Ala
ENST00000371953.7:c.778_779delinsGC	ENSP00000361021.3:p.Lys260Ala
ENST00000472832.2:c.205_206delinsGC	ENSP00000483066.1:p.Lys69Ala
NM_000314.5:c.778_779delinsGC	NP_000305.3:p.Lys260Ala
NM_000314.6:c.778_779delinsGC	NP_000305.3:p.Lys260Ala
NM_001304717.2:c.1297_1298delinsGC	NP_001291646.2:p.Lys433Ala
NM_001304718.1:c.187_188delinsGC	NP_001291647.1:p.Lys63Ala
XM_006717926.2:c.733_734delinsGC	XP_006717989.1:p.Lys245Ala
XM_011539981.1:c.778_779delinsGC	XP_011538283.1:p.Lys260Ala
XM_011539982.1:c.682_683delinsGC	XP_011538284.1:p.Lys228Ala
XR_945791.1:n.1348_1349delinsGC
NM_000314.7:c.778_779delinsGC	NP_000305.3:p.Lys260Ala
NM_001304717.5:c.1297_1298delinsGC	NP_001291646.4:p.Lys433Ala
NM_001304718.2:c.187_188delinsGC	NP_001291647.1:p.Lys63Ala
NM_000314.8:c.778_779delinsGC MANE Select	NP_000305.3:p.Lys260Ala