Canonical Allele Identifier: CA669574404

Gene: PTEN

Linked Data

• dbSNP Id: rs1410799404
• MyVariant Identifiers: chr10:g.87966915_87966916insTTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87966917_87966918insGTT , CM000672.2:g.87966917_87966918insGTT	GRCh38
NC_000010.10:g.89726674_89726675insGTT , CM000672.1:g.89726674_89726675insGTT	GRCh37
NC_000010.9:g.89716654_89716655insGTT	NCBI36
NG_007466.2:g.108479_108480insGTT , LRG_311:g.108479_108480insGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710265.1:c.*1686_*1687insGTT	ENSP00000518161.1:n.*1686_*1687insGTT
ENST00000688158.2:n.3392_3393insGTT
ENST00000706954.1:c.*1445_*1446insGTT	ENSP00000516674.1:n.*1445_*1446insGTT
ENST00000706955.1:c.*2692_*2693insGTT	ENSP00000516675.1:n.*2692_*2693insGTT
ENST00000688158.1:c.*2768_*2769insGTT	ENSP00000509254.1:n.*2768_*2769insGTT
ENST00000693560.1:c.*1445_*1446insGTT	ENSP00000509861.1:n.*1445_*1446insGTT
ENST00000371953.8:c.*1445_*1446insGTT MANE Select	ENSP00000361021.3:n.*1445_*1446insGTT
ENST00000371953.7:c.*1445_*1446insGTT	ENSP00000361021.3:n.*1445_*1446insGTT
NM_000314.5:c.*1445_*1446insGTT	NP_000305.3:n.*1445_*1446insGTT
NM_000314.6:c.*1445_*1446insGTT	NP_000305.3:n.*1445_*1446insGTT
NM_001304717.2:c.*1445_*1446insGTT	NP_001291646.2:n.*1445_*1446insGTT
NM_001304718.1:c.*1445_*1446insGTT	NP_001291647.1:n.*1445_*1446insGTT
XM_006717926.2:c.*1445_*1446insGTT	XP_006717989.1:n.*1445_*1446insGTT
XM_011539982.1:c.*1445_*1446insGTT	XP_011538284.1:n.*1445_*1446insGTT
XR_945791.1:n.3227_3228insGTT
NM_000314.7:c.*1445_*1446insGTT	NP_000305.3:n.*1445_*1446insGTT
NM_001304717.5:c.*1445_*1446insGTT	NP_001291646.4:n.*1445_*1446insGTT
NM_001304718.2:c.*1445_*1446insGTT	NP_001291647.1:n.*1445_*1446insGTT
NM_000314.8:c.*1445_*1446insGTT MANE Select	NP_000305.3:n.*1445_*1446insGTT