Canonical Allele Identifier: CA2505901655

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87966918_87966919insGT , CM000672.2:g.87966918_87966919insGT	GRCh38
NC_000010.10:g.89726675_89726676insGT , CM000672.1:g.89726675_89726676insGT	GRCh37
NC_000010.9:g.89716655_89716656insGT	NCBI36
NG_007466.2:g.108480_108481insGT , LRG_311:g.108480_108481insGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710265.1:c.*1687_*1688insGT	ENSP00000518161.1:n.*1687_*1688insGT
ENST00000688158.2:n.3393_3394insGT
ENST00000706954.1:c.*1446_*1447insGT	ENSP00000516674.1:n.*1446_*1447insGT
ENST00000706955.1:c.*2693_*2694insGT	ENSP00000516675.1:n.*2693_*2694insGT
ENST00000688158.1:c.*2769_*2770insGT	ENSP00000509254.1:n.*2769_*2770insGT
ENST00000693560.1:c.*1446_*1447insGT	ENSP00000509861.1:n.*1446_*1447insGT
ENST00000371953.8:c.*1446_*1447insGT MANE Select	ENSP00000361021.3:n.*1446_*1447insGT
ENST00000371953.7:c.*1446_*1447insGT	ENSP00000361021.3:n.*1446_*1447insGT
NM_000314.5:c.*1446_*1447insGT	NP_000305.3:n.*1446_*1447insGT
NM_000314.6:c.*1446_*1447insGT	NP_000305.3:n.*1446_*1447insGT
NM_001304717.2:c.*1446_*1447insGT	NP_001291646.2:n.*1446_*1447insGT
NM_001304718.1:c.*1446_*1447insGT	NP_001291647.1:n.*1446_*1447insGT
XM_006717926.2:c.*1446_*1447insGT	XP_006717989.1:n.*1446_*1447insGT
XM_011539982.1:c.*1446_*1447insGT	XP_011538284.1:n.*1446_*1447insGT
XR_945791.1:n.3228_3229insGT
NM_000314.7:c.*1446_*1447insGT	NP_000305.3:n.*1446_*1447insGT
NM_001304717.5:c.*1446_*1447insGT	NP_001291646.4:n.*1446_*1447insGT
NM_001304718.2:c.*1446_*1447insGT	NP_001291647.1:n.*1446_*1447insGT
NM_000314.8:c.*1446_*1447insGT MANE Select	NP_000305.3:n.*1446_*1447insGT