Canonical Allele Identifier: CA1926175801

Gene: PTEN

Linked Data

• dbSNP Id: rs1860778358

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87966908_87966909insGTTT , CM000672.2:g.87966908_87966909insGTTT	GRCh38
NC_000010.10:g.89726665_89726666insGTTT , CM000672.1:g.89726665_89726666insGTTT	GRCh37
NC_000010.9:g.89716645_89716646insGTTT	NCBI36
NG_007466.2:g.108470_108471insGTTT , LRG_311:g.108470_108471insGTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710265.1:c.*1677_*1678insGTTT	ENSP00000518161.1:n.*1677_*1678insGTTT
ENST00000688158.2:n.3383_3384insGTTT
ENST00000706954.1:c.*1436_*1437insGTTT	ENSP00000516674.1:n.*1436_*1437insGTTT
ENST00000706955.1:c.*2683_*2684insGTTT	ENSP00000516675.1:n.*2683_*2684insGTTT
ENST00000688158.1:c.*2759_*2760insGTTT	ENSP00000509254.1:n.*2759_*2760insGTTT
ENST00000693560.1:c.*1436_*1437insGTTT	ENSP00000509861.1:n.*1436_*1437insGTTT
ENST00000371953.8:c.*1436_*1437insGTTT MANE Select	ENSP00000361021.3:n.*1436_*1437insGTTT
ENST00000371953.7:c.*1436_*1437insGTTT	ENSP00000361021.3:n.*1436_*1437insGTTT
NM_000314.5:c.*1436_*1437insGTTT	NP_000305.3:n.*1436_*1437insGTTT
NM_000314.6:c.*1436_*1437insGTTT	NP_000305.3:n.*1436_*1437insGTTT
NM_001304717.2:c.*1436_*1437insGTTT	NP_001291646.2:n.*1436_*1437insGTTT
NM_001304718.1:c.*1436_*1437insGTTT	NP_001291647.1:n.*1436_*1437insGTTT
XM_006717926.2:c.*1436_*1437insGTTT	XP_006717989.1:n.*1436_*1437insGTTT
XM_011539982.1:c.*1436_*1437insGTTT	XP_011538284.1:n.*1436_*1437insGTTT
XR_945791.1:n.3218_3219insGTTT
NM_000314.7:c.*1436_*1437insGTTT	NP_000305.3:n.*1436_*1437insGTTT
NM_001304717.5:c.*1436_*1437insGTTT	NP_001291646.4:n.*1436_*1437insGTTT
NM_001304718.2:c.*1436_*1437insGTTT	NP_001291647.1:n.*1436_*1437insGTTT
NM_000314.8:c.*1436_*1437insGTTT MANE Select	NP_000305.3:n.*1436_*1437insGTTT