Canonical Allele Identifier: CA1926175907

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87966929_87966932delinsTTTA , CM000672.2:g.87966929_87966932delinsTTTA	GRCh38
NC_000010.10:g.89726686_89726689delinsTTTA , CM000672.1:g.89726686_89726689delinsTTTA	GRCh37
NC_000010.9:g.89716666_89716669delinsTTTA	NCBI36
NG_007466.2:g.108491_108494delinsTTTA , LRG_311:g.108491_108494delinsTTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710265.1:c.*1698_*1701delinsTTTA	ENSP00000518161.1:n.*1698_*1701delinsTTTA
ENST00000688158.2:n.3404_3407delinsTTTA
ENST00000706954.1:c.*1457_*1460delinsTTTA	ENSP00000516674.1:n.*1457_*1460delinsTTTA
ENST00000706955.1:c.*2704_*2707delinsTTTA	ENSP00000516675.1:n.*2704_*2707delinsTTTA
ENST00000688158.1:c.*2780_*2783delinsTTTA	ENSP00000509254.1:n.*2780_*2783delinsTTTA
ENST00000693560.1:c.*1457_*1460delinsTTTA	ENSP00000509861.1:n.*1457_*1460delinsTTTA
ENST00000371953.8:c.*1457_*1460delinsTTTA MANE Select	ENSP00000361021.3:n.*1457_*1460delinsTTTA
ENST00000371953.7:c.*1457_*1460delinsTTTA	ENSP00000361021.3:n.*1457_*1460delinsTTTA
NM_000314.5:c.*1457_*1460delinsTTTA	NP_000305.3:n.*1457_*1460delinsTTTA
NM_000314.6:c.*1457_*1460delinsTTTA	NP_000305.3:n.*1457_*1460delinsTTTA
NM_001304717.2:c.*1457_*1460delinsTTTA	NP_001291646.2:n.*1457_*1460delinsTTTA
NM_001304718.1:c.*1457_*1460delinsTTTA	NP_001291647.1:n.*1457_*1460delinsTTTA
XM_006717926.2:c.*1457_*1460delinsTTTA	XP_006717989.1:n.*1457_*1460delinsTTTA
XM_011539982.1:c.*1457_*1460delinsTTTA	XP_011538284.1:n.*1457_*1460delinsTTTA
XR_945791.1:n.3239_3242delinsTTTA
NM_000314.7:c.*1457_*1460delinsTTTA	NP_000305.3:n.*1457_*1460delinsTTTA
NM_001304717.5:c.*1457_*1460delinsTTTA	NP_001291646.4:n.*1457_*1460delinsTTTA
NM_001304718.2:c.*1457_*1460delinsTTTA	NP_001291647.1:n.*1457_*1460delinsTTTA
NM_000314.8:c.*1457_*1460delinsTTTA MANE Select	NP_000305.3:n.*1457_*1460delinsTTTA