Canonical Allele Identifier: CA1926175918

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87966931_87966932delinsTA , CM000672.2:g.87966931_87966932delinsTA	GRCh38
NC_000010.10:g.89726688_89726689delinsTA , CM000672.1:g.89726688_89726689delinsTA	GRCh37
NC_000010.9:g.89716668_89716669delinsTA	NCBI36
NG_007466.2:g.108493_108494delinsTA , LRG_311:g.108493_108494delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710265.1:c.*1700_*1701delinsTA	ENSP00000518161.1:n.*1700_*1701delinsTA
ENST00000688158.2:n.3406_3407delinsTA
ENST00000706954.1:c.*1459_*1460delinsTA	ENSP00000516674.1:n.*1459_*1460delinsTA
ENST00000706955.1:c.*2706_*2707delinsTA	ENSP00000516675.1:n.*2706_*2707delinsTA
ENST00000688158.1:c.*2782_*2783delinsTA	ENSP00000509254.1:n.*2782_*2783delinsTA
ENST00000693560.1:c.*1459_*1460delinsTA	ENSP00000509861.1:n.*1459_*1460delinsTA
ENST00000371953.8:c.*1459_*1460delinsTA MANE Select	ENSP00000361021.3:n.*1459_*1460delinsTA
ENST00000371953.7:c.*1459_*1460delinsTA	ENSP00000361021.3:n.*1459_*1460delinsTA
NM_000314.5:c.*1459_*1460delinsTA	NP_000305.3:n.*1459_*1460delinsTA
NM_000314.6:c.*1459_*1460delinsTA	NP_000305.3:n.*1459_*1460delinsTA
NM_001304717.2:c.*1459_*1460delinsTA	NP_001291646.2:n.*1459_*1460delinsTA
NM_001304718.1:c.*1459_*1460delinsTA	NP_001291647.1:n.*1459_*1460delinsTA
XM_006717926.2:c.*1459_*1460delinsTA	XP_006717989.1:n.*1459_*1460delinsTA
XM_011539982.1:c.*1459_*1460delinsTA	XP_011538284.1:n.*1459_*1460delinsTA
XR_945791.1:n.3241_3242delinsTA
NM_000314.7:c.*1459_*1460delinsTA	NP_000305.3:n.*1459_*1460delinsTA
NM_001304717.5:c.*1459_*1460delinsTA	NP_001291646.4:n.*1459_*1460delinsTA
NM_001304718.2:c.*1459_*1460delinsTA	NP_001291647.1:n.*1459_*1460delinsTA
NM_000314.8:c.*1459_*1460delinsTA MANE Select	NP_000305.3:n.*1459_*1460delinsTA