Canonical Allele Identifier: CA891835514

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960981_87960983delinsATG , CM000672.2:g.87960981_87960983delinsATG	GRCh38
NC_000010.10:g.89720738_89720740delinsATG , CM000672.1:g.89720738_89720740delinsATG	GRCh37
NC_000010.9:g.89710718_89710720delinsATG	NCBI36
NG_007466.2:g.102543_102545delinsATG , LRG_311:g.102543_102545delinsATG

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.982_984delinsATG	ENSP00000514759.2:p.Asp328Met
ENST00000710265.1:c.889_891delinsATG	ENSP00000518161.1:p.Asp297Met
ENST00000472832.3:c.889_891delinsATG	ENSP00000483066.2:p.Asp297Met
ENST00000688158.2:n.1624_1626delinsATG
ENST00000688922.2:c.*719_*721delinsATG	ENSP00000508742.2:n.*719_*721delinsATG
ENST00000700021.1:c.844_846delinsATG	ENSP00000514757.1:p.Asp282Met
ENST00000700022.1:c.*228_*230delinsATG	ENSP00000514758.1:n.*228_*230delinsATG
ENST00000700023.1:n.2047_2049delinsATG
ENST00000700024.1:n.2281_2283delinsATG
ENST00000700025.1:n.1658_1660delinsATG
ENST00000700026.1:n.526_528delinsATG
ENST00000706954.1:c.889_891delinsATG	ENSP00000516674.1:p.Asp297Met
ENST00000706955.1:c.*924_*926delinsATG	ENSP00000516675.1:n.*924_*926delinsATG
ENST00000686459.1:c.*475_*477delinsATG	ENSP00000508909.1:n.*475_*477delinsATG
ENST00000688158.1:c.*1000_*1002delinsATG	ENSP00000509254.1:n.*1000_*1002delinsATG
ENST00000688308.1:c.889_891delinsATG	ENSP00000508752.1:p.Asp297Met
ENST00000688922.1:c.810_812delinsATG
ENST00000693560.1:c.1408_1410delinsATG	ENSP00000509861.1:p.Asp470Met
ENST00000371953.8:c.889_891delinsATG MANE Select	ENSP00000361021.3:p.Asp297Met
ENST00000371953.7:c.889_891delinsATG	ENSP00000361021.3:p.Asp297Met
ENST00000472832.2:c.316_318delinsATG	ENSP00000483066.1:p.Asp106Met
NM_000314.5:c.889_891delinsATG	NP_000305.3:p.Asp297Met
NM_000314.6:c.889_891delinsATG	NP_000305.3:p.Asp297Met
NM_001304717.2:c.1408_1410delinsATG	NP_001291646.2:p.Asp470Met
NM_001304718.1:c.298_300delinsATG	NP_001291647.1:p.Asp100Met
XM_006717926.2:c.844_846delinsATG	XP_006717989.1:p.Asp282Met
XM_011539981.1:c.889_891delinsATG	XP_011538283.1:p.Asp297Met
XM_011539982.1:c.793_795delinsATG	XP_011538284.1:p.Asp265Met
XR_945791.1:n.1459_1461delinsATG
NM_000314.7:c.889_891delinsATG	NP_000305.3:p.Asp297Met
NM_001304717.5:c.1408_1410delinsATG	NP_001291646.4:p.Asp470Met
NM_001304718.2:c.298_300delinsATG	NP_001291647.1:p.Asp100Met
NM_000314.8:c.889_891delinsATG MANE Select	NP_000305.3:p.Asp297Met