Canonical Allele Identifier: CA653764234

Gene: PTEN

Linked Data

• COSMIC: COSN15839116

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965484_87965485insG , CM000672.2:g.87965484_87965485insG	GRCh38
NC_000010.10:g.89725241_89725242insG , CM000672.1:g.89725241_89725242insG	GRCh37
NC_000010.9:g.89715221_89715222insG	NCBI36
NG_007466.2:g.107046_107047insG , LRG_311:g.107046_107047insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.*12_*13insG	ENSP00000514759.2:n.*12_*13insG
ENST00000710265.1:c.*253_*254insG	ENSP00000518161.1:n.*253_*254insG
ENST00000688158.2:n.1959_1960insG
ENST00000688922.2:c.*1054_*1055insG	ENSP00000508742.2:n.*1054_*1055insG
ENST00000700021.1:c.*12_*13insG	ENSP00000514757.1:n.*12_*13insG
ENST00000700022.1:c.*563_*564insG	ENSP00000514758.1:n.*563_*564insG
ENST00000700023.1:n.2382_2383insG
ENST00000700024.1:n.2616_2617insG
ENST00000706954.1:c.*12_*13insG	ENSP00000516674.1:n.*12_*13insG
ENST00000706955.1:c.*1259_*1260insG	ENSP00000516675.1:n.*1259_*1260insG
ENST00000686459.1:c.*810_*811insG	ENSP00000508909.1:n.*810_*811insG
ENST00000688158.1:c.*1335_*1336insG	ENSP00000509254.1:n.*1335_*1336insG
ENST00000688308.1:c.*12_*13insG	ENSP00000508752.1:n.*12_*13insG
ENST00000688922.1:c.1145_1146insG
ENST00000693560.1:c.*12_*13insG	ENSP00000509861.1:n.*12_*13insG
ENST00000371953.8:c.*12_*13insG MANE Select	ENSP00000361021.3:n.*12_*13insG
ENST00000371953.7:c.*12_*13insG	ENSP00000361021.3:n.*12_*13insG
NM_000314.5:c.*12_*13insG	NP_000305.3:n.*12_*13insG
NM_000314.6:c.*12_*13insG	NP_000305.3:n.*12_*13insG
NM_001304717.2:c.*12_*13insG	NP_001291646.2:n.*12_*13insG
NM_001304718.1:c.*12_*13insG	NP_001291647.1:n.*12_*13insG
XM_006717926.2:c.*12_*13insG	XP_006717989.1:n.*12_*13insG
XM_011539982.1:c.*12_*13insG	XP_011538284.1:n.*12_*13insG
XR_945791.1:n.1794_1795insG
NM_000314.7:c.*12_*13insG	NP_000305.3:n.*12_*13insG
NM_001304717.5:c.*12_*13insG	NP_001291646.4:n.*12_*13insG
NM_001304718.2:c.*12_*13insG	NP_001291647.1:n.*12_*13insG
NM_000314.8:c.*12_*13insG MANE Select	NP_000305.3:n.*12_*13insG