Canonical Allele Identifier: CA1926174127

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965473_87965474delinsAT , CM000672.2:g.87965473_87965474delinsAT	GRCh38
NC_000010.10:g.89725230_89725231delinsAT , CM000672.1:g.89725230_89725231delinsAT	GRCh37
NC_000010.9:g.89715210_89715211delinsAT	NCBI36
NG_007466.2:g.107035_107036delinsAT , LRG_311:g.107035_107036delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.*1_*2delinsAT	ENSP00000514759.2:n.*1_*2delinsAT
ENST00000710265.1:c.*242_*243delinsAT	ENSP00000518161.1:n.*242_*243delinsAT
ENST00000688158.2:n.1948_1949delinsAT
ENST00000688922.2:c.*1043_*1044delinsAT	ENSP00000508742.2:n.*1043_*1044delinsAT
ENST00000700021.1:c.*1_*2delinsAT	ENSP00000514757.1:n.*1_*2delinsAT
ENST00000700022.1:c.*552_*553delinsAT	ENSP00000514758.1:n.*552_*553delinsAT
ENST00000700023.1:n.2371_2372delinsAT
ENST00000700024.1:n.2605_2606delinsAT
ENST00000706954.1:c.*1_*2delinsAT	ENSP00000516674.1:n.*1_*2delinsAT
ENST00000706955.1:c.*1248_*1249delinsAT	ENSP00000516675.1:n.*1248_*1249delinsAT
ENST00000686459.1:c.*799_*800delinsAT	ENSP00000508909.1:n.*799_*800delinsAT
ENST00000688158.1:c.*1324_*1325delinsAT	ENSP00000509254.1:n.*1324_*1325delinsAT
ENST00000688308.1:c.*1_*2delinsAT	ENSP00000508752.1:n.*1_*2delinsAT
ENST00000688922.1:c.1134_1135delinsAT
ENST00000693560.1:c.*1_*2delinsAT	ENSP00000509861.1:n.*1_*2delinsAT
ENST00000371953.8:c.*1_*2delinsAT MANE Select	ENSP00000361021.3:n.*1_*2delinsAT
ENST00000371953.7:c.*1_*2delinsAT	ENSP00000361021.3:n.*1_*2delinsAT
NM_000314.5:c.*1_*2delinsAT	NP_000305.3:n.*1_*2delinsAT
NM_000314.6:c.*1_*2delinsAT	NP_000305.3:n.*1_*2delinsAT
NM_001304717.2:c.*1_*2delinsAT	NP_001291646.2:n.*1_*2delinsAT
NM_001304718.1:c.*1_*2delinsAT	NP_001291647.1:n.*1_*2delinsAT
XM_006717926.2:c.*1_*2delinsAT	XP_006717989.1:n.*1_*2delinsAT
XM_011539982.1:c.*1_*2delinsAT	XP_011538284.1:n.*1_*2delinsAT
XR_945791.1:n.1783_1784delinsAT
NM_000314.7:c.*1_*2delinsAT	NP_000305.3:n.*1_*2delinsAT
NM_001304717.5:c.*1_*2delinsAT	NP_001291646.4:n.*1_*2delinsAT
NM_001304718.2:c.*1_*2delinsAT	NP_001291647.1:n.*1_*2delinsAT
NM_000314.8:c.*1_*2delinsAT MANE Select	NP_000305.3:n.*1_*2delinsAT