Canonical Allele Identifier: CA669574212

Gene: PTEN

Linked Data

• dbSNP Id: rs1289761417
• gnomAD v3: 10-87966836-GAC-G
• gnomAD v4: 10-87966836-GAC-G
• MyVariant Identifiers: chr10:g.87966837_87966838del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87966838_87966839del , CM000672.2:g.87966838_87966839del	GRCh38
NC_000010.10:g.89726595_89726596del , CM000672.1:g.89726595_89726596del	GRCh37
NC_000010.9:g.89716575_89716576del	NCBI36
NG_007466.2:g.108400_108401del , LRG_311:g.108400_108401del

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.*1366_*1367del	ENSP00000514759.2:n.*1366_*1367del
ENST00000710265.1:c.*1607_*1608del	ENSP00000518161.1:n.*1607_*1608del
ENST00000688158.2:n.3313_3314del
ENST00000688922.2:c.*2408_*2409del	ENSP00000508742.2:n.*2408_*2409del
ENST00000700021.1:c.*1366_*1367del	ENSP00000514757.1:n.*1366_*1367del
ENST00000700024.1:n.3970_3971del
ENST00000706954.1:c.*1366_*1367del	ENSP00000516674.1:n.*1366_*1367del
ENST00000706955.1:c.*2613_*2614del	ENSP00000516675.1:n.*2613_*2614del
ENST00000688158.1:c.*2689_*2690del	ENSP00000509254.1:n.*2689_*2690del
ENST00000688308.1:c.*1366_*1367del	ENSP00000508752.1:n.*1366_*1367del
ENST00000688922.1:c.2499_2500del
ENST00000693560.1:c.*1366_*1367del	ENSP00000509861.1:n.*1366_*1367del
ENST00000371953.8:c.*1366_*1367del MANE Select	ENSP00000361021.3:n.*1366_*1367del
ENST00000371953.7:c.*1366_*1367del	ENSP00000361021.3:n.*1366_*1367del
NM_000314.5:c.*1366_*1367del	NP_000305.3:n.*1366_*1367del
NM_000314.6:c.*1366_*1367del	NP_000305.3:n.*1366_*1367del
NM_001304717.2:c.*1366_*1367del	NP_001291646.2:n.*1366_*1367del
NM_001304718.1:c.*1366_*1367del	NP_001291647.1:n.*1366_*1367del
XM_006717926.2:c.*1366_*1367del	XP_006717989.1:n.*1366_*1367del
XM_011539982.1:c.*1366_*1367del	XP_011538284.1:n.*1366_*1367del
XR_945791.1:n.3148_3149del
NM_000314.7:c.*1366_*1367del	NP_000305.3:n.*1366_*1367del
NM_001304717.5:c.*1366_*1367del	NP_001291646.4:n.*1366_*1367del
NM_001304718.2:c.*1366_*1367del	NP_001291647.1:n.*1366_*1367del
NM_000314.8:c.*1366_*1367del MANE Select	NP_000305.3:n.*1366_*1367del