Canonical Allele Identifier: CA645554082

Gene: PTEN

Linked Data

• COSMIC: COSM5876

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960912_87961115del , CM000672.2:g.87960912_87961115del	GRCh38
NC_000010.10:g.89720669_89720872del , CM000672.1:g.89720669_89720872del	GRCh37
NC_000010.9:g.89710649_89710852del	NCBI36
NG_007466.2:g.102474_102677del , LRG_311:g.102474_102677del

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.913_1116del	ENSP00000514759.2:p.Trp305_Phe372del
ENST00000710265.1:c.820_1023del	ENSP00000518161.1:p.Trp274_Phe341del
ENST00000472832.3:c.820_1023del	ENSP00000483066.2:p.Trp274_Phe341del
ENST00000688158.2:n.1555_1758del
ENST00000688922.2:c.*650_*853del	ENSP00000508742.2:n.*650_*853del
ENST00000700021.1:c.775_978del	ENSP00000514757.1:p.Trp259_Phe326del
ENST00000700022.1:c.*159_*362del	ENSP00000514758.1:n.*159_*362del
ENST00000700023.1:n.1978_2181del
ENST00000700024.1:n.2212_2415del
ENST00000700025.1:n.1589_1792del
ENST00000700026.1:n.457_660del
ENST00000706954.1:c.820_1023del	ENSP00000516674.1:p.Trp274_Phe341del
ENST00000706955.1:c.*855_*1058del	ENSP00000516675.1:n.*855_*1058del
ENST00000686459.1:c.*406_*609del	ENSP00000508909.1:n.*406_*609del
ENST00000688158.1:c.*931_*1134del	ENSP00000509254.1:n.*931_*1134del
ENST00000688308.1:c.820_1023del	ENSP00000508752.1:p.Trp274_Phe341del
ENST00000688922.1:c.741_944del
ENST00000693560.1:c.1339_1542del	ENSP00000509861.1:p.Trp447_Phe514del
ENST00000371953.8:c.820_1023del MANE Select	ENSP00000361021.3:p.Trp274_Phe341del
ENST00000371953.7:c.820_1023del	ENSP00000361021.3:p.Trp274_Phe341del
ENST00000472832.2:c.247_450del	ENSP00000483066.1:p.Trp83_Phe150del
NM_000314.5:c.820_1023del	NP_000305.3:p.Trp274_Phe341del
NM_000314.6:c.820_1023del	NP_000305.3:p.Trp274_Phe341del
NM_001304717.2:c.1339_1542del	NP_001291646.2:p.Trp447_Phe514del
NM_001304718.1:c.229_432del	NP_001291647.1:p.Trp77_Phe144del
XM_006717926.2:c.775_978del	XP_006717989.1:p.Trp259_Phe326del
XM_011539981.1:c.820_1023del	XP_011538283.1:p.Trp274_Phe341del
XM_011539982.1:c.724_927del	XP_011538284.1:p.Trp242_Phe309del
XR_945791.1:n.1390_1593del
NM_000314.7:c.820_1023del	NP_000305.3:p.Trp274_Phe341del
NM_001304717.5:c.1339_1542del	NP_001291646.4:p.Trp447_Phe514del
NM_001304718.2:c.229_432del	NP_001291647.1:p.Trp77_Phe144del
NM_000314.8:c.820_1023del MANE Select	NP_000305.3:p.Trp274_Phe341del