Canonical Allele Identifier: CA1926175699

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87966902_87966918delinsGTTTTTTTTTTTTTTTT , CM000672.2:g.87966902_87966918delinsGTTTTTTTTTTTTTTTT	GRCh38
NC_000010.10:g.89726659_89726675delinsGTTTTTTTTTTTTTTTT , CM000672.1:g.89726659_89726675delinsGTTTTTTTTTTTTTTTT	GRCh37
NC_000010.9:g.89716639_89716655delinsGTTTTTTTTTTTTTTTT	NCBI36
NG_007466.2:g.108464_108480delinsGTTTTTTTTTTTTTTTT , LRG_311:g.108464_108480delinsGTTTTTTTTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000710265.1:c.*1671_*1687delinsGTTTTTTTTTTTTTTTT	ENSP00000518161.1:n.*1671_*1687delinsGTTT...
ENST00000688158.2:n.3377_3393delinsGTTTTTTTTTTTTTTTT
ENST00000706954.1:c.*1430_*1446delinsGTTTTTTTTTTTTTTTT	ENSP00000516674.1:n.*1430_*1446delinsGTTT...
ENST00000706955.1:c.*2677_*2693delinsGTTTTTTTTTTTTTTTT	ENSP00000516675.1:n.*2677_*2693delinsGTTT...
ENST00000688158.1:c.*2753_*2769delinsGTTTTTTTTTTTTTTTT	ENSP00000509254.1:n.*2753_*2769delinsGTTT...
ENST00000693560.1:c.*1430_*1446delinsGTTTTTTTTTTTTTTTT	ENSP00000509861.1:n.*1430_*1446delinsGTTT...
ENST00000371953.8:c.*1430_*1446delinsGTTTTTTTTTTTTTTTT MANE Select	ENSP00000361021.3:n.*1430_*1446delinsGTTT...
ENST00000371953.7:c.*1430_*1446delinsGTTTTTTTTTTTTTTTT	ENSP00000361021.3:n.*1430_*1446delinsGTTT...
NM_000314.5:c.*1430_*1446delinsGTTTTTTTTTTTTTTTT	NP_000305.3:n.*1430_*1446delinsGTTTTTTTTT...
NM_000314.6:c.*1430_*1446delinsGTTTTTTTTTTTTTTTT	NP_000305.3:n.*1430_*1446delinsGTTTTTTTTT...
NM_001304717.2:c.*1430_*1446delinsGTTTTTTTTTTTTTTTT	NP_001291646.2:n.*1430_*1446delinsGTTTTTT...
NM_001304718.1:c.*1430_*1446delinsGTTTTTTTTTTTTTTTT	NP_001291647.1:n.*1430_*1446delinsGTTTTTT...
XM_006717926.2:c.*1430_*1446delinsGTTTTTTTTTTTTTTTT	XP_006717989.1:n.*1430_*1446delinsGTTTTTT...
XM_011539982.1:c.*1430_*1446delinsGTTTTTTTTTTTTTTTT	XP_011538284.1:n.*1430_*1446delinsGTTTTTT...
XR_945791.1:n.3212_3228delinsGTTTTTTTTTTTTTTTT
NM_000314.7:c.*1430_*1446delinsGTTTTTTTTTTTTTTTT	NP_000305.3:n.*1430_*1446delinsGTTTTTTTTT...
NM_001304717.5:c.*1430_*1446delinsGTTTTTTTTTTTTTTTT	NP_001291646.4:n.*1430_*1446delinsGTTTTTT...
NM_001304718.2:c.*1430_*1446delinsGTTTTTTTTTTTTTTTT	NP_001291647.1:n.*1430_*1446delinsGTTTTTT...
NM_000314.8:c.*1430_*1446delinsGTTTTTTTTTTTTTTTT MANE Select	NP_000305.3:n.*1430_*1446delinsGTTTTTTTTT...