Canonical Allele Identifier: CA930910719

Gene: PTEN

Linked Data

• gnomAD v3: 10-87966902-G-GTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTATTGTTT
• gnomAD v4: 10-87966902-G-GTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTATTGTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87966931_87966932insTTTATTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT , CM000672.2:g.87966931_87966932insTTTATTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	GRCh38
NC_000010.10:g.89726688_89726689insTTTATTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT , CM000672.1:g.89726688_89726689insTTTATTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	GRCh37
NC_000010.9:g.89716668_89716669insTTTATTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NCBI36
NG_007466.2:g.108493_108494insTTTATTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT , LRG_311:g.108493_108494insTTTATTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000710265.1:c.*1700_*1701insTTTATTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000518161.1:n.*1700_*1701insTTTATTG...
ENST00000688158.2:n.3406_3407insTTTATTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000706954.1:c.*1459_*1460insTTTATTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000516674.1:n.*1459_*1460insTTTATTG...
ENST00000706955.1:c.*2706_*2707insTTTATTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000516675.1:n.*2706_*2707insTTTATTG...
ENST00000688158.1:c.*2782_*2783insTTTATTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000509254.1:n.*2782_*2783insTTTATTG...
ENST00000693560.1:c.*1459_*1460insTTTATTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000509861.1:n.*1459_*1460insTTTATTG...
ENST00000371953.8:c.*1459_*1460insTTTATTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select	ENSP00000361021.3:n.*1459_*1460insTTTATTG...
ENST00000371953.7:c.*1459_*1460insTTTATTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000361021.3:n.*1459_*1460insTTTATTG...
NM_000314.5:c.*1459_*1460insTTTATTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NP_000305.3:n.*1459_*1460insTTTATTGTTTTTT...
NM_000314.6:c.*1459_*1460insTTTATTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NP_000305.3:n.*1459_*1460insTTTATTGTTTTTT...
NM_001304717.2:c.*1459_*1460insTTTATTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NP_001291646.2:n.*1459_*1460insTTTATTGTTT...
NM_001304718.1:c.*1459_*1460insTTTATTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NP_001291647.1:n.*1459_*1460insTTTATTGTTT...
XM_006717926.2:c.*1459_*1460insTTTATTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_006717989.1:n.*1459_*1460insTTTATTGTTT...
XM_011539982.1:c.*1459_*1460insTTTATTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_011538284.1:n.*1459_*1460insTTTATTGTTT...
XR_945791.1:n.3241_3242insTTTATTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
NM_000314.7:c.*1459_*1460insTTTATTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NP_000305.3:n.*1459_*1460insTTTATTGTTTTTT...
NM_001304717.5:c.*1459_*1460insTTTATTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NP_001291646.4:n.*1459_*1460insTTTATTGTTT...
NM_001304718.2:c.*1459_*1460insTTTATTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NP_001291647.1:n.*1459_*1460insTTTATTGTTT...
NM_000314.8:c.*1459_*1460insTTTATTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select	NP_000305.3:n.*1459_*1460insTTTATTGTTTTTT...