Canonical Allele Identifier: CA1926175624

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87966838_87966840delinsCAT , CM000672.2:g.87966838_87966840delinsCAT	GRCh38
NC_000010.10:g.89726595_89726597delinsCAT , CM000672.1:g.89726595_89726597delinsCAT	GRCh37
NC_000010.9:g.89716575_89716577delinsCAT	NCBI36
NG_007466.2:g.108400_108402delinsCAT , LRG_311:g.108400_108402delinsCAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.*1366_*1368delinsCAT	ENSP00000514759.2:n.*1366_*1368delinsCAT
ENST00000710265.1:c.*1607_*1609delinsCAT	ENSP00000518161.1:n.*1607_*1609delinsCAT
ENST00000688158.2:n.3313_3315delinsCAT
ENST00000688922.2:c.*2408_*2410delinsCAT	ENSP00000508742.2:n.*2408_*2410delinsCAT
ENST00000700021.1:c.*1366_*1368delinsCAT	ENSP00000514757.1:n.*1366_*1368delinsCAT
ENST00000700024.1:n.3970_3972delinsCAT
ENST00000706954.1:c.*1366_*1368delinsCAT	ENSP00000516674.1:n.*1366_*1368delinsCAT
ENST00000706955.1:c.*2613_*2615delinsCAT	ENSP00000516675.1:n.*2613_*2615delinsCAT
ENST00000688158.1:c.*2689_*2691delinsCAT	ENSP00000509254.1:n.*2689_*2691delinsCAT
ENST00000688308.1:c.*1366_*1368delinsCAT	ENSP00000508752.1:n.*1366_*1368delinsCAT
ENST00000688922.1:c.2499_2501delinsCAT
ENST00000693560.1:c.*1366_*1368delinsCAT	ENSP00000509861.1:n.*1366_*1368delinsCAT
ENST00000371953.8:c.*1366_*1368delinsCAT MANE Select	ENSP00000361021.3:n.*1366_*1368delinsCAT
ENST00000371953.7:c.*1366_*1368delinsCAT	ENSP00000361021.3:n.*1366_*1368delinsCAT
NM_000314.5:c.*1366_*1368delinsCAT	NP_000305.3:n.*1366_*1368delinsCAT
NM_000314.6:c.*1366_*1368delinsCAT	NP_000305.3:n.*1366_*1368delinsCAT
NM_001304717.2:c.*1366_*1368delinsCAT	NP_001291646.2:n.*1366_*1368delinsCAT
NM_001304718.1:c.*1366_*1368delinsCAT	NP_001291647.1:n.*1366_*1368delinsCAT
XM_006717926.2:c.*1366_*1368delinsCAT	XP_006717989.1:n.*1366_*1368delinsCAT
XM_011539982.1:c.*1366_*1368delinsCAT	XP_011538284.1:n.*1366_*1368delinsCAT
XR_945791.1:n.3148_3150delinsCAT
NM_000314.7:c.*1366_*1368delinsCAT	NP_000305.3:n.*1366_*1368delinsCAT
NM_001304717.5:c.*1366_*1368delinsCAT	NP_001291646.4:n.*1366_*1368delinsCAT
NM_001304718.2:c.*1366_*1368delinsCAT	NP_001291647.1:n.*1366_*1368delinsCAT
NM_000314.8:c.*1366_*1368delinsCAT MANE Select	NP_000305.3:n.*1366_*1368delinsCAT