Canonical Allele Identifier: CA891836718

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961065_87961067delinsATG , CM000672.2:g.87961065_87961067delinsATG	GRCh38
NC_000010.10:g.89720822_89720824delinsATG , CM000672.1:g.89720822_89720824delinsATG	GRCh37
NC_000010.9:g.89710802_89710804delinsATG	NCBI36
NG_007466.2:g.102627_102629delinsATG , LRG_311:g.102627_102629delinsATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1066_1068delinsATG	ENSP00000514759.2:p.Leu356Met
ENST00000710265.1:c.973_975delinsATG	ENSP00000518161.1:p.Leu325Met
ENST00000472832.3:c.973_975delinsATG	ENSP00000483066.2:p.Leu325Met
ENST00000688158.2:n.1708_1710delinsATG
ENST00000688922.2:c.*803_*805delinsATG	ENSP00000508742.2:n.*803_*805delinsATG
ENST00000700021.1:c.928_930delinsATG	ENSP00000514757.1:p.Leu310Met
ENST00000700022.1:c.*312_*314delinsATG	ENSP00000514758.1:n.*312_*314delinsATG
ENST00000700023.1:n.2131_2133delinsATG
ENST00000700024.1:n.2365_2367delinsATG
ENST00000700025.1:n.1742_1744delinsATG
ENST00000700026.1:n.610_612delinsATG
ENST00000706954.1:c.973_975delinsATG	ENSP00000516674.1:p.Leu325Met
ENST00000706955.1:c.*1008_*1010delinsATG	ENSP00000516675.1:n.*1008_*1010delinsATG
ENST00000686459.1:c.*559_*561delinsATG	ENSP00000508909.1:n.*559_*561delinsATG
ENST00000688158.1:c.*1084_*1086delinsATG	ENSP00000509254.1:n.*1084_*1086delinsATG
ENST00000688308.1:c.973_975delinsATG	ENSP00000508752.1:p.Leu325Met
ENST00000688922.1:c.894_896delinsATG
ENST00000693560.1:c.1492_1494delinsATG	ENSP00000509861.1:p.Leu498Met
ENST00000371953.8:c.973_975delinsATG MANE Select	ENSP00000361021.3:p.Leu325Met
ENST00000371953.7:c.973_975delinsATG	ENSP00000361021.3:p.Leu325Met
ENST00000472832.2:c.400_402delinsATG	ENSP00000483066.1:p.Leu134Met
NM_000314.5:c.973_975delinsATG	NP_000305.3:p.Leu325Met
NM_000314.6:c.973_975delinsATG	NP_000305.3:p.Leu325Met
NM_001304717.2:c.1492_1494delinsATG	NP_001291646.2:p.Leu498Met
NM_001304718.1:c.382_384delinsATG	NP_001291647.1:p.Leu128Met
XM_006717926.2:c.928_930delinsATG	XP_006717989.1:p.Leu310Met
XM_011539981.1:c.973_975delinsATG	XP_011538283.1:p.Leu325Met
XM_011539982.1:c.877_879delinsATG	XP_011538284.1:p.Leu293Met
XR_945791.1:n.1543_1545delinsATG
NM_000314.7:c.973_975delinsATG	NP_000305.3:p.Leu325Met
NM_001304717.5:c.1492_1494delinsATG	NP_001291646.4:p.Leu498Met
NM_001304718.2:c.382_384delinsATG	NP_001291647.1:p.Leu128Met
NM_000314.8:c.973_975delinsATG MANE Select	NP_000305.3:p.Leu325Met