Canonical Allele Identifier: CA891835669

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960987_87960989delinsATG , CM000672.2:g.87960987_87960989delinsATG	GRCh38
NC_000010.10:g.89720744_89720746delinsATG , CM000672.1:g.89720744_89720746delinsATG	GRCh37
NC_000010.9:g.89710724_89710726delinsATG	NCBI36
NG_007466.2:g.102549_102551delinsATG , LRG_311:g.102549_102551delinsATG

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.988_990delinsATG	ENSP00000514759.2:p.Glu330Met
ENST00000710265.1:c.895_897delinsATG	ENSP00000518161.1:p.Glu299Met
ENST00000472832.3:c.895_897delinsATG	ENSP00000483066.2:p.Glu299Met
ENST00000688158.2:n.1630_1632delinsATG
ENST00000688922.2:c.*725_*727delinsATG	ENSP00000508742.2:n.*725_*727delinsATG
ENST00000700021.1:c.850_852delinsATG	ENSP00000514757.1:p.Glu284Met
ENST00000700022.1:c.*234_*236delinsATG	ENSP00000514758.1:n.*234_*236delinsATG
ENST00000700023.1:n.2053_2055delinsATG
ENST00000700024.1:n.2287_2289delinsATG
ENST00000700025.1:n.1664_1666delinsATG
ENST00000700026.1:n.532_534delinsATG
ENST00000706954.1:c.895_897delinsATG	ENSP00000516674.1:p.Glu299Met
ENST00000706955.1:c.*930_*932delinsATG	ENSP00000516675.1:n.*930_*932delinsATG
ENST00000686459.1:c.*481_*483delinsATG	ENSP00000508909.1:n.*481_*483delinsATG
ENST00000688158.1:c.*1006_*1008delinsATG	ENSP00000509254.1:n.*1006_*1008delinsATG
ENST00000688308.1:c.895_897delinsATG	ENSP00000508752.1:p.Glu299Met
ENST00000688922.1:c.816_818delinsATG
ENST00000693560.1:c.1414_1416delinsATG	ENSP00000509861.1:p.Glu472Met
ENST00000371953.8:c.895_897delinsATG MANE Select	ENSP00000361021.3:p.Glu299Met
ENST00000371953.7:c.895_897delinsATG	ENSP00000361021.3:p.Glu299Met
ENST00000472832.2:c.322_324delinsATG	ENSP00000483066.1:p.Glu108Met
NM_000314.5:c.895_897delinsATG	NP_000305.3:p.Glu299Met
NM_000314.6:c.895_897delinsATG	NP_000305.3:p.Glu299Met
NM_001304717.2:c.1414_1416delinsATG	NP_001291646.2:p.Glu472Met
NM_001304718.1:c.304_306delinsATG	NP_001291647.1:p.Glu102Met
XM_006717926.2:c.850_852delinsATG	XP_006717989.1:p.Glu284Met
XM_011539981.1:c.895_897delinsATG	XP_011538283.1:p.Glu299Met
XM_011539982.1:c.799_801delinsATG	XP_011538284.1:p.Glu267Met
XR_945791.1:n.1465_1467delinsATG
NM_000314.7:c.895_897delinsATG	NP_000305.3:p.Glu299Met
NM_001304717.5:c.1414_1416delinsATG	NP_001291646.4:p.Glu472Met
NM_001304718.2:c.304_306delinsATG	NP_001291647.1:p.Glu102Met
NM_000314.8:c.895_897delinsATG MANE Select	NP_000305.3:p.Glu299Met