Canonical Allele Identifier: CA669574342

Gene: PTEN

Linked Data

• dbSNP Id: rs1337812221
• gnomAD v3: 10-87966904-T-TG
• gnomAD v4: 10-87966904-T-TG
• MyVariant Identifiers: chr10:g.87966904_87966905insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87966904_87966905insG , CM000672.2:g.87966904_87966905insG	GRCh38
NC_000010.10:g.89726661_89726662insG , CM000672.1:g.89726661_89726662insG	GRCh37
NC_000010.9:g.89716641_89716642insG	NCBI36
NG_007466.2:g.108466_108467insG , LRG_311:g.108466_108467insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710265.1:c.*1673_*1674insG	ENSP00000518161.1:n.*1673_*1674insG
ENST00000688158.2:n.3379_3380insG
ENST00000706954.1:c.*1432_*1433insG	ENSP00000516674.1:n.*1432_*1433insG
ENST00000706955.1:c.*2679_*2680insG	ENSP00000516675.1:n.*2679_*2680insG
ENST00000688158.1:c.*2755_*2756insG	ENSP00000509254.1:n.*2755_*2756insG
ENST00000693560.1:c.*1432_*1433insG	ENSP00000509861.1:n.*1432_*1433insG
ENST00000371953.8:c.*1432_*1433insG MANE Select	ENSP00000361021.3:n.*1432_*1433insG
ENST00000371953.7:c.*1432_*1433insG	ENSP00000361021.3:n.*1432_*1433insG
NM_000314.5:c.*1432_*1433insG	NP_000305.3:n.*1432_*1433insG
NM_000314.6:c.*1432_*1433insG	NP_000305.3:n.*1432_*1433insG
NM_001304717.2:c.*1432_*1433insG	NP_001291646.2:n.*1432_*1433insG
NM_001304718.1:c.*1432_*1433insG	NP_001291647.1:n.*1432_*1433insG
XM_006717926.2:c.*1432_*1433insG	XP_006717989.1:n.*1432_*1433insG
XM_011539982.1:c.*1432_*1433insG	XP_011538284.1:n.*1432_*1433insG
XR_945791.1:n.3214_3215insG
NM_000314.7:c.*1432_*1433insG	NP_000305.3:n.*1432_*1433insG
NM_001304717.5:c.*1432_*1433insG	NP_001291646.4:n.*1432_*1433insG
NM_001304718.2:c.*1432_*1433insG	NP_001291647.1:n.*1432_*1433insG
NM_000314.8:c.*1432_*1433insG MANE Select	NP_000305.3:n.*1432_*1433insG