Canonical Allele Identifier: CA891840146

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960894_87960896delinsAGA , CM000672.2:g.87960894_87960896delinsAGA	GRCh38
NC_000010.10:g.89720651_89720653delinsAGA , CM000672.1:g.89720651_89720653delinsAGA	GRCh37
NC_000010.9:g.89710631_89710633delinsAGA	NCBI36
NG_007466.2:g.102456_102458delinsAGA , LRG_311:g.102456_102458delinsAGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.895_897delinsAGA	ENSP00000514759.2:p.Asp299Arg
ENST00000710265.1:c.802_804delinsAGA	ENSP00000518161.1:p.Asp268Arg
ENST00000472832.3:c.802_804delinsAGA	ENSP00000483066.2:p.Asp268Arg
ENST00000688158.2:n.1537_1539delinsAGA
ENST00000688922.2:c.*632_*634delinsAGA	ENSP00000508742.2:n.*632_*634delinsAGA
ENST00000700021.1:c.757_759delinsAGA	ENSP00000514757.1:p.Asp253Arg
ENST00000700022.1:c.*141_*143delinsAGA	ENSP00000514758.1:n.*141_*143delinsAGA
ENST00000700023.1:n.1960_1962delinsAGA
ENST00000700024.1:n.2194_2196delinsAGA
ENST00000700025.1:n.1571_1573delinsAGA
ENST00000700026.1:n.439_441delinsAGA
ENST00000700029.1:c.729_731delinsAGA
ENST00000706954.1:c.802_804delinsAGA	ENSP00000516674.1:p.Asp268Arg
ENST00000706955.1:c.*837_*839delinsAGA	ENSP00000516675.1:n.*837_*839delinsAGA
ENST00000686459.1:c.*388_*390delinsAGA	ENSP00000508909.1:n.*388_*390delinsAGA
ENST00000688158.1:c.*913_*915delinsAGA	ENSP00000509254.1:n.*913_*915delinsAGA
ENST00000688308.1:c.802_804delinsAGA	ENSP00000508752.1:p.Asp268Arg
ENST00000688922.1:c.723_725delinsAGA
ENST00000693560.1:c.1321_1323delinsAGA	ENSP00000509861.1:p.Asp441Arg
ENST00000371953.8:c.802_804delinsAGA MANE Select	ENSP00000361021.3:p.Asp268Arg
ENST00000371953.7:c.802_804delinsAGA	ENSP00000361021.3:p.Asp268Arg
ENST00000472832.2:c.229_231delinsAGA	ENSP00000483066.1:p.Asp77Arg
NM_000314.5:c.802_804delinsAGA	NP_000305.3:p.Asp268Arg
NM_000314.6:c.802_804delinsAGA	NP_000305.3:p.Asp268Arg
NM_001304717.2:c.1321_1323delinsAGA	NP_001291646.2:p.Asp441Arg
NM_001304718.1:c.211_213delinsAGA	NP_001291647.1:p.Asp71Arg
XM_006717926.2:c.757_759delinsAGA	XP_006717989.1:p.Asp253Arg
XM_011539981.1:c.802_804delinsAGA	XP_011538283.1:p.Asp268Arg
XM_011539982.1:c.706_708delinsAGA	XP_011538284.1:p.Asp236Arg
XR_945791.1:n.1372_1374delinsAGA
NM_000314.7:c.802_804delinsAGA	NP_000305.3:p.Asp268Arg
NM_001304717.5:c.1321_1323delinsAGA	NP_001291646.4:p.Asp441Arg
NM_001304718.2:c.211_213delinsAGA	NP_001291647.1:p.Asp71Arg
NM_000314.8:c.802_804delinsAGA MANE Select	NP_000305.3:p.Asp268Arg