Canonical Allele Identifier: CA930910744

Gene: PTEN

Linked Data

• dbSNP Id: rs1860778159
• gnomAD v3: 10-87966904-T-TTG
• gnomAD v4: 10-87966904-T-TTG

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87966905_87966906insGT , CM000672.2:g.87966905_87966906insGT	GRCh38
NC_000010.10:g.89726662_89726663insGT , CM000672.1:g.89726662_89726663insGT	GRCh37
NC_000010.9:g.89716642_89716643insGT	NCBI36
NG_007466.2:g.108467_108468insGT , LRG_311:g.108467_108468insGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710265.1:c.*1674_*1675insGT	ENSP00000518161.1:n.*1674_*1675insGT
ENST00000688158.2:n.3380_3381insGT
ENST00000706954.1:c.*1433_*1434insGT	ENSP00000516674.1:n.*1433_*1434insGT
ENST00000706955.1:c.*2680_*2681insGT	ENSP00000516675.1:n.*2680_*2681insGT
ENST00000688158.1:c.*2756_*2757insGT	ENSP00000509254.1:n.*2756_*2757insGT
ENST00000693560.1:c.*1433_*1434insGT	ENSP00000509861.1:n.*1433_*1434insGT
ENST00000371953.8:c.*1433_*1434insGT MANE Select	ENSP00000361021.3:n.*1433_*1434insGT
ENST00000371953.7:c.*1433_*1434insGT	ENSP00000361021.3:n.*1433_*1434insGT
NM_000314.5:c.*1433_*1434insGT	NP_000305.3:n.*1433_*1434insGT
NM_000314.6:c.*1433_*1434insGT	NP_000305.3:n.*1433_*1434insGT
NM_001304717.2:c.*1433_*1434insGT	NP_001291646.2:n.*1433_*1434insGT
NM_001304718.1:c.*1433_*1434insGT	NP_001291647.1:n.*1433_*1434insGT
XM_006717926.2:c.*1433_*1434insGT	XP_006717989.1:n.*1433_*1434insGT
XM_011539982.1:c.*1433_*1434insGT	XP_011538284.1:n.*1433_*1434insGT
XR_945791.1:n.3215_3216insGT
NM_000314.7:c.*1433_*1434insGT	NP_000305.3:n.*1433_*1434insGT
NM_001304717.5:c.*1433_*1434insGT	NP_001291646.4:n.*1433_*1434insGT
NM_001304718.2:c.*1433_*1434insGT	NP_001291647.1:n.*1433_*1434insGT
NM_000314.8:c.*1433_*1434insGT MANE Select	NP_000305.3:n.*1433_*1434insGT