Canonical Allele Identifier: CA1926177219

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87967732_87967735delinsGTTA , CM000672.2:g.87967732_87967735delinsGTTA	GRCh38
NC_000010.10:g.89727489_89727492delinsGTTA , CM000672.1:g.89727489_89727492delinsGTTA	GRCh37
NC_000010.9:g.89717469_89717472delinsGTTA	NCBI36
NG_007466.2:g.109294_109297delinsGTTA , LRG_311:g.109294_109297delinsGTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710265.1:c.*2501_*2504delinsGTTA	ENSP00000518161.1:n.*2501_*2504delinsGTTA
ENST00000688158.2:n.4207_4210delinsGTTA
ENST00000706954.1:c.*2260_*2263delinsGTTA	ENSP00000516674.1:n.*2260_*2263delinsGTTA
ENST00000706955.1:c.*3507_*3510delinsGTTA	ENSP00000516675.1:n.*3507_*3510delinsGTTA
ENST00000688158.1:c.*3583_*3586delinsGTTA	ENSP00000509254.1:n.*3583_*3586delinsGTTA
ENST00000693560.1:c.*2260_*2263delinsGTTA	ENSP00000509861.1:n.*2260_*2263delinsGTTA
ENST00000371953.8:c.*2260_*2263delinsGTTA MANE Select	ENSP00000361021.3:n.*2260_*2263delinsGTTA
ENST00000371953.7:c.*2260_*2263delinsGTTA	ENSP00000361021.3:n.*2260_*2263delinsGTTA
NM_000314.5:c.*2260_*2263delinsGTTA	NP_000305.3:n.*2260_*2263delinsGTTA
NM_000314.6:c.*2260_*2263delinsGTTA	NP_000305.3:n.*2260_*2263delinsGTTA
NM_001304717.2:c.*2260_*2263delinsGTTA	NP_001291646.2:n.*2260_*2263delinsGTTA
NM_001304718.1:c.*2260_*2263delinsGTTA	NP_001291647.1:n.*2260_*2263delinsGTTA
XM_006717926.2:c.*2260_*2263delinsGTTA	XP_006717989.1:n.*2260_*2263delinsGTTA
XM_011539982.1:c.*2260_*2263delinsGTTA	XP_011538284.1:n.*2260_*2263delinsGTTA
XR_945791.1:n.4042_4045delinsGTTA
NM_000314.7:c.*2260_*2263delinsGTTA	NP_000305.3:n.*2260_*2263delinsGTTA
NM_001304717.5:c.*2260_*2263delinsGTTA	NP_001291646.4:n.*2260_*2263delinsGTTA
NM_001304718.2:c.*2260_*2263delinsGTTA	NP_001291647.1:n.*2260_*2263delinsGTTA
NM_000314.8:c.*2260_*2263delinsGTTA MANE Select	NP_000305.3:n.*2260_*2263delinsGTTA