Canonical Allele Identifier: CA1926175849

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87966915_87966932delinsTTTTTTTTTTTTTTTTTA , CM000672.2:g.87966915_87966932delinsTTTTTTTTTTTTTTTTTA	GRCh38
NC_000010.10:g.89726672_89726689delinsTTTTTTTTTTTTTTTTTA , CM000672.1:g.89726672_89726689delinsTTTTTTTTTTTTTTTTTA	GRCh37
NC_000010.9:g.89716652_89716669delinsTTTTTTTTTTTTTTTTTA	NCBI36
NG_007466.2:g.108477_108494delinsTTTTTTTTTTTTTTTTTA , LRG_311:g.108477_108494delinsTTTTTTTTTTTTTTTTTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000710265.1:c.*1684_*1701delinsTTTTTTTTTTTTTTTTTA	ENSP00000518161.1:n.*1684_*1701delinsTTTTTTTTTTTTTTTTTA
ENST00000688158.2:n.3390_3407delinsTTTTTTTTTTTTTTTTTA
ENST00000706954.1:c.*1443_*1460delinsTTTTTTTTTTTTTTTTTA	ENSP00000516674.1:n.*1443_*1460delinsTTTTTTTTTTTTTTTTTA
ENST00000706955.1:c.*2690_*2707delinsTTTTTTTTTTTTTTTTTA	ENSP00000516675.1:n.*2690_*2707delinsTTTTTTTTTTTTTTTTTA
ENST00000688158.1:c.*2766_*2783delinsTTTTTTTTTTTTTTTTTA	ENSP00000509254.1:n.*2766_*2783delinsTTTTTTTTTTTTTTTTTA
ENST00000693560.1:c.*1443_*1460delinsTTTTTTTTTTTTTTTTTA	ENSP00000509861.1:n.*1443_*1460delinsTTTTTTTTTTTTTTTTTA
ENST00000371953.8:c.*1443_*1460delinsTTTTTTTTTTTTTTTTTA MANE Select	ENSP00000361021.3:n.*1443_*1460delinsTTTTTTTTTTTTTTTTTA
ENST00000371953.7:c.*1443_*1460delinsTTTTTTTTTTTTTTTTTA	ENSP00000361021.3:n.*1443_*1460delinsTTTTTTTTTTTTTTTTTA
NM_000314.5:c.*1443_*1460delinsTTTTTTTTTTTTTTTTTA	NP_000305.3:n.*1443_*1460delinsTTTTTTTTTTTTTTTTTA
NM_000314.6:c.*1443_*1460delinsTTTTTTTTTTTTTTTTTA	NP_000305.3:n.*1443_*1460delinsTTTTTTTTTTTTTTTTTA
NM_001304717.2:c.*1443_*1460delinsTTTTTTTTTTTTTTTTTA	NP_001291646.2:n.*1443_*1460delinsTTTTTTTTTTTTTTTTTA
NM_001304718.1:c.*1443_*1460delinsTTTTTTTTTTTTTTTTTA	NP_001291647.1:n.*1443_*1460delinsTTTTTTTTTTTTTTTTTA
XM_006717926.2:c.*1443_*1460delinsTTTTTTTTTTTTTTTTTA	XP_006717989.1:n.*1443_*1460delinsTTTTTTTTTTTTTTTTTA
XM_011539982.1:c.*1443_*1460delinsTTTTTTTTTTTTTTTTTA	XP_011538284.1:n.*1443_*1460delinsTTTTTTTTTTTTTTTTTA
XR_945791.1:n.3225_3242delinsTTTTTTTTTTTTTTTTTA
NM_000314.7:c.*1443_*1460delinsTTTTTTTTTTTTTTTTTA	NP_000305.3:n.*1443_*1460delinsTTTTTTTTTTTTTTTTTA
NM_001304717.5:c.*1443_*1460delinsTTTTTTTTTTTTTTTTTA	NP_001291646.4:n.*1443_*1460delinsTTTTTTTTTTTTTTTTTA
NM_001304718.2:c.*1443_*1460delinsTTTTTTTTTTTTTTTTTA	NP_001291647.1:n.*1443_*1460delinsTTTTTTTTTTTTTTTTTA
NM_000314.8:c.*1443_*1460delinsTTTTTTTTTTTTTTTTTA MANE Select	NP_000305.3:n.*1443_*1460delinsTTTTTTTTTTTTTTTTTA