Canonical Allele Identifier: CA1926175621

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87966836_87966838delinsGAC , CM000672.2:g.87966836_87966838delinsGAC	GRCh38
NC_000010.10:g.89726593_89726595delinsGAC , CM000672.1:g.89726593_89726595delinsGAC	GRCh37
NC_000010.9:g.89716573_89716575delinsGAC	NCBI36
NG_007466.2:g.108398_108400delinsGAC , LRG_311:g.108398_108400delinsGAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.*1364_*1366delinsGAC	ENSP00000514759.2:n.*1364_*1366delinsGAC
ENST00000710265.1:c.*1605_*1607delinsGAC	ENSP00000518161.1:n.*1605_*1607delinsGAC
ENST00000688158.2:n.3311_3313delinsGAC
ENST00000688922.2:c.*2406_*2408delinsGAC	ENSP00000508742.2:n.*2406_*2408delinsGAC
ENST00000700021.1:c.*1364_*1366delinsGAC	ENSP00000514757.1:n.*1364_*1366delinsGAC
ENST00000700024.1:n.3968_3970delinsGAC
ENST00000706954.1:c.*1364_*1366delinsGAC	ENSP00000516674.1:n.*1364_*1366delinsGAC
ENST00000706955.1:c.*2611_*2613delinsGAC	ENSP00000516675.1:n.*2611_*2613delinsGAC
ENST00000688158.1:c.*2687_*2689delinsGAC	ENSP00000509254.1:n.*2687_*2689delinsGAC
ENST00000688308.1:c.*1364_*1366delinsGAC	ENSP00000508752.1:n.*1364_*1366delinsGAC
ENST00000688922.1:c.2497_2499delinsGAC
ENST00000693560.1:c.*1364_*1366delinsGAC	ENSP00000509861.1:n.*1364_*1366delinsGAC
ENST00000371953.8:c.*1364_*1366delinsGAC MANE Select	ENSP00000361021.3:n.*1364_*1366delinsGAC
ENST00000371953.7:c.*1364_*1366delinsGAC	ENSP00000361021.3:n.*1364_*1366delinsGAC
NM_000314.5:c.*1364_*1366delinsGAC	NP_000305.3:n.*1364_*1366delinsGAC
NM_000314.6:c.*1364_*1366delinsGAC	NP_000305.3:n.*1364_*1366delinsGAC
NM_001304717.2:c.*1364_*1366delinsGAC	NP_001291646.2:n.*1364_*1366delinsGAC
NM_001304718.1:c.*1364_*1366delinsGAC	NP_001291647.1:n.*1364_*1366delinsGAC
XM_006717926.2:c.*1364_*1366delinsGAC	XP_006717989.1:n.*1364_*1366delinsGAC
XM_011539982.1:c.*1364_*1366delinsGAC	XP_011538284.1:n.*1364_*1366delinsGAC
XR_945791.1:n.3146_3148delinsGAC
NM_000314.7:c.*1364_*1366delinsGAC	NP_000305.3:n.*1364_*1366delinsGAC
NM_001304717.5:c.*1364_*1366delinsGAC	NP_001291646.4:n.*1364_*1366delinsGAC
NM_001304718.2:c.*1364_*1366delinsGAC	NP_001291647.1:n.*1364_*1366delinsGAC
NM_000314.8:c.*1364_*1366delinsGAC MANE Select	NP_000305.3:n.*1364_*1366delinsGAC