Canonical Allele Identifier: CA930910903

Gene: PTEN

Linked Data

• gnomAD v3: 10-87966932-A-ATTTTT
• gnomAD v4: 10-87966932-A-ATTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87966932_87966933insTTTTT , CM000672.2:g.87966932_87966933insTTTTT	GRCh38
NC_000010.10:g.89726689_89726690insTTTTT , CM000672.1:g.89726689_89726690insTTTTT	GRCh37
NC_000010.9:g.89716669_89716670insTTTTT	NCBI36
NG_007466.2:g.108494_108495insTTTTT , LRG_311:g.108494_108495insTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710265.1:c.*1701_*1702insTTTTT	ENSP00000518161.1:n.*1701_*1702insTTTTT
ENST00000688158.2:n.3407_3408insTTTTT
ENST00000706954.1:c.*1460_*1461insTTTTT	ENSP00000516674.1:n.*1460_*1461insTTTTT
ENST00000706955.1:c.*2707_*2708insTTTTT	ENSP00000516675.1:n.*2707_*2708insTTTTT
ENST00000688158.1:c.*2783_*2784insTTTTT	ENSP00000509254.1:n.*2783_*2784insTTTTT
ENST00000693560.1:c.*1460_*1461insTTTTT	ENSP00000509861.1:n.*1460_*1461insTTTTT
ENST00000371953.8:c.*1460_*1461insTTTTT MANE Select	ENSP00000361021.3:n.*1460_*1461insTTTTT
ENST00000371953.7:c.*1460_*1461insTTTTT	ENSP00000361021.3:n.*1460_*1461insTTTTT
NM_000314.5:c.*1460_*1461insTTTTT	NP_000305.3:n.*1460_*1461insTTTTT
NM_000314.6:c.*1460_*1461insTTTTT	NP_000305.3:n.*1460_*1461insTTTTT
NM_001304717.2:c.*1460_*1461insTTTTT	NP_001291646.2:n.*1460_*1461insTTTTT
NM_001304718.1:c.*1460_*1461insTTTTT	NP_001291647.1:n.*1460_*1461insTTTTT
XM_006717926.2:c.*1460_*1461insTTTTT	XP_006717989.1:n.*1460_*1461insTTTTT
XM_011539982.1:c.*1460_*1461insTTTTT	XP_011538284.1:n.*1460_*1461insTTTTT
XR_945791.1:n.3242_3243insTTTTT
NM_000314.7:c.*1460_*1461insTTTTT	NP_000305.3:n.*1460_*1461insTTTTT
NM_001304717.5:c.*1460_*1461insTTTTT	NP_001291646.4:n.*1460_*1461insTTTTT
NM_001304718.2:c.*1460_*1461insTTTTT	NP_001291647.1:n.*1460_*1461insTTTTT
NM_000314.8:c.*1460_*1461insTTTTT MANE Select	NP_000305.3:n.*1460_*1461insTTTTT