Canonical Allele Identifier: CA1926175888

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87966922_87966932delinsTTTTTTTTTTA , CM000672.2:g.87966922_87966932delinsTTTTTTTTTTA	GRCh38
NC_000010.10:g.89726679_89726689delinsTTTTTTTTTTA , CM000672.1:g.89726679_89726689delinsTTTTTTTTTTA	GRCh37
NC_000010.9:g.89716659_89716669delinsTTTTTTTTTTA	NCBI36
NG_007466.2:g.108484_108494delinsTTTTTTTTTTA , LRG_311:g.108484_108494delinsTTTTTTTTTTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000710265.1:c.*1691_*1701delinsTTTTTTTTTTA	ENSP00000518161.1:n.*1691_*1701delinsTTTTTTTTTTA
ENST00000688158.2:n.3397_3407delinsTTTTTTTTTTA
ENST00000706954.1:c.*1450_*1460delinsTTTTTTTTTTA	ENSP00000516674.1:n.*1450_*1460delinsTTTTTTTTTTA
ENST00000706955.1:c.*2697_*2707delinsTTTTTTTTTTA	ENSP00000516675.1:n.*2697_*2707delinsTTTTTTTTTTA
ENST00000688158.1:c.*2773_*2783delinsTTTTTTTTTTA	ENSP00000509254.1:n.*2773_*2783delinsTTTTTTTTTTA
ENST00000693560.1:c.*1450_*1460delinsTTTTTTTTTTA	ENSP00000509861.1:n.*1450_*1460delinsTTTTTTTTTTA
ENST00000371953.8:c.*1450_*1460delinsTTTTTTTTTTA MANE Select	ENSP00000361021.3:n.*1450_*1460delinsTTTTTTTTTTA
ENST00000371953.7:c.*1450_*1460delinsTTTTTTTTTTA	ENSP00000361021.3:n.*1450_*1460delinsTTTTTTTTTTA
NM_000314.5:c.*1450_*1460delinsTTTTTTTTTTA	NP_000305.3:n.*1450_*1460delinsTTTTTTTTTTA
NM_000314.6:c.*1450_*1460delinsTTTTTTTTTTA	NP_000305.3:n.*1450_*1460delinsTTTTTTTTTTA
NM_001304717.2:c.*1450_*1460delinsTTTTTTTTTTA	NP_001291646.2:n.*1450_*1460delinsTTTTTTTTTTA
NM_001304718.1:c.*1450_*1460delinsTTTTTTTTTTA	NP_001291647.1:n.*1450_*1460delinsTTTTTTTTTTA
XM_006717926.2:c.*1450_*1460delinsTTTTTTTTTTA	XP_006717989.1:n.*1450_*1460delinsTTTTTTTTTTA
XM_011539982.1:c.*1450_*1460delinsTTTTTTTTTTA	XP_011538284.1:n.*1450_*1460delinsTTTTTTTTTTA
XR_945791.1:n.3232_3242delinsTTTTTTTTTTA
NM_000314.7:c.*1450_*1460delinsTTTTTTTTTTA	NP_000305.3:n.*1450_*1460delinsTTTTTTTTTTA
NM_001304717.5:c.*1450_*1460delinsTTTTTTTTTTA	NP_001291646.4:n.*1450_*1460delinsTTTTTTTTTTA
NM_001304718.2:c.*1450_*1460delinsTTTTTTTTTTA	NP_001291647.1:n.*1450_*1460delinsTTTTTTTTTTA
NM_000314.8:c.*1450_*1460delinsTTTTTTTTTTA MANE Select	NP_000305.3:n.*1450_*1460delinsTTTTTTTTTTA