Canonical Allele Identifier: CA2588954344

Gene: PTEN

Linked Data

• gnomAD v3: 10-87966919-T-TTG
• gnomAD v4: 10-87966919-T-TTG

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87966920_87966921insGT , CM000672.2:g.87966920_87966921insGT	GRCh38
NC_000010.10:g.89726677_89726678insGT , CM000672.1:g.89726677_89726678insGT	GRCh37
NC_000010.9:g.89716657_89716658insGT	NCBI36
NG_007466.2:g.108482_108483insGT , LRG_311:g.108482_108483insGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710265.1:c.*1689_*1690insGT	ENSP00000518161.1:n.*1689_*1690insGT
ENST00000688158.2:n.3395_3396insGT
ENST00000706954.1:c.*1448_*1449insGT	ENSP00000516674.1:n.*1448_*1449insGT
ENST00000706955.1:c.*2695_*2696insGT	ENSP00000516675.1:n.*2695_*2696insGT
ENST00000688158.1:c.*2771_*2772insGT	ENSP00000509254.1:n.*2771_*2772insGT
ENST00000693560.1:c.*1448_*1449insGT	ENSP00000509861.1:n.*1448_*1449insGT
ENST00000371953.8:c.*1448_*1449insGT MANE Select	ENSP00000361021.3:n.*1448_*1449insGT
ENST00000371953.7:c.*1448_*1449insGT	ENSP00000361021.3:n.*1448_*1449insGT
NM_000314.5:c.*1448_*1449insGT	NP_000305.3:n.*1448_*1449insGT
NM_000314.6:c.*1448_*1449insGT	NP_000305.3:n.*1448_*1449insGT
NM_001304717.2:c.*1448_*1449insGT	NP_001291646.2:n.*1448_*1449insGT
NM_001304718.1:c.*1448_*1449insGT	NP_001291647.1:n.*1448_*1449insGT
XM_006717926.2:c.*1448_*1449insGT	XP_006717989.1:n.*1448_*1449insGT
XM_011539982.1:c.*1448_*1449insGT	XP_011538284.1:n.*1448_*1449insGT
XR_945791.1:n.3230_3231insGT
NM_000314.7:c.*1448_*1449insGT	NP_000305.3:n.*1448_*1449insGT
NM_001304717.5:c.*1448_*1449insGT	NP_001291646.4:n.*1448_*1449insGT
NM_001304718.2:c.*1448_*1449insGT	NP_001291647.1:n.*1448_*1449insGT
NM_000314.8:c.*1448_*1449insGT MANE Select	NP_000305.3:n.*1448_*1449insGT