Canonical Allele Identifier: CA930910955

Gene: PTEN

Linked Data

• gnomAD v3: 10-87966934-A-ATTTTTT
• gnomAD v4: 10-87966934-A-ATTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87966935_87966936insTTTTTT , CM000672.2:g.87966935_87966936insTTTTTT	GRCh38
NC_000010.10:g.89726692_89726693insTTTTTT , CM000672.1:g.89726692_89726693insTTTTTT	GRCh37
NC_000010.9:g.89716672_89716673insTTTTTT	NCBI36
NG_007466.2:g.108497_108498insTTTTTT , LRG_311:g.108497_108498insTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710265.1:c.*1704_*1705insTTTTTT	ENSP00000518161.1:n.*1704_*1705insTTTTTT
ENST00000688158.2:n.3410_3411insTTTTTT
ENST00000706954.1:c.*1463_*1464insTTTTTT	ENSP00000516674.1:n.*1463_*1464insTTTTTT
ENST00000706955.1:c.*2710_*2711insTTTTTT	ENSP00000516675.1:n.*2710_*2711insTTTTTT
ENST00000688158.1:c.*2786_*2787insTTTTTT	ENSP00000509254.1:n.*2786_*2787insTTTTTT
ENST00000693560.1:c.*1463_*1464insTTTTTT	ENSP00000509861.1:n.*1463_*1464insTTTTTT
ENST00000371953.8:c.*1463_*1464insTTTTTT MANE Select	ENSP00000361021.3:n.*1463_*1464insTTTTTT
ENST00000371953.7:c.*1463_*1464insTTTTTT	ENSP00000361021.3:n.*1463_*1464insTTTTTT
NM_000314.5:c.*1463_*1464insTTTTTT	NP_000305.3:n.*1463_*1464insTTTTTT
NM_000314.6:c.*1463_*1464insTTTTTT	NP_000305.3:n.*1463_*1464insTTTTTT
NM_001304717.2:c.*1463_*1464insTTTTTT	NP_001291646.2:n.*1463_*1464insTTTTTT
NM_001304718.1:c.*1463_*1464insTTTTTT	NP_001291647.1:n.*1463_*1464insTTTTTT
XM_006717926.2:c.*1463_*1464insTTTTTT	XP_006717989.1:n.*1463_*1464insTTTTTT
XM_011539982.1:c.*1463_*1464insTTTTTT	XP_011538284.1:n.*1463_*1464insTTTTTT
XR_945791.1:n.3245_3246insTTTTTT
NM_000314.7:c.*1463_*1464insTTTTTT	NP_000305.3:n.*1463_*1464insTTTTTT
NM_001304717.5:c.*1463_*1464insTTTTTT	NP_001291646.4:n.*1463_*1464insTTTTTT
NM_001304718.2:c.*1463_*1464insTTTTTT	NP_001291647.1:n.*1463_*1464insTTTTTT
NM_000314.8:c.*1463_*1464insTTTTTT MANE Select	NP_000305.3:n.*1463_*1464insTTTTTT