Canonical Allele Identifier: CA891836806

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961074_87961075delinsAG , CM000672.2:g.87961074_87961075delinsAG	GRCh38
NC_000010.10:g.89720831_89720832delinsAG , CM000672.1:g.89720831_89720832delinsAG	GRCh37
NC_000010.9:g.89710811_89710812delinsAG	NCBI36
NG_007466.2:g.102636_102637delinsAG , LRG_311:g.102636_102637delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1075_1076delinsAG	ENSP00000514759.2:p.Ala359Arg
ENST00000710265.1:c.982_983delinsAG	ENSP00000518161.1:p.Ala328Arg
ENST00000472832.3:c.982_983delinsAG	ENSP00000483066.2:p.Ala328Arg
ENST00000688158.2:n.1717_1718delinsAG
ENST00000688922.2:c.*812_*813delinsAG	ENSP00000508742.2:n.*812_*813delinsAG
ENST00000700021.1:c.937_938delinsAG	ENSP00000514757.1:p.Ala313Arg
ENST00000700022.1:c.*321_*322delinsAG	ENSP00000514758.1:n.*321_*322delinsAG
ENST00000700023.1:n.2140_2141delinsAG
ENST00000700024.1:n.2374_2375delinsAG
ENST00000700025.1:n.1751_1752delinsAG
ENST00000700026.1:n.619_620delinsAG
ENST00000706954.1:c.982_983delinsAG	ENSP00000516674.1:p.Ala328Arg
ENST00000706955.1:c.*1017_*1018delinsAG	ENSP00000516675.1:n.*1017_*1018delinsAG
ENST00000686459.1:c.*568_*569delinsAG	ENSP00000508909.1:n.*568_*569delinsAG
ENST00000688158.1:c.*1093_*1094delinsAG	ENSP00000509254.1:n.*1093_*1094delinsAG
ENST00000688308.1:c.982_983delinsAG	ENSP00000508752.1:p.Ala328Arg
ENST00000688922.1:c.903_904delinsAG
ENST00000693560.1:c.1501_1502delinsAG	ENSP00000509861.1:p.Ala501Arg
ENST00000371953.8:c.982_983delinsAG MANE Select	ENSP00000361021.3:p.Ala328Arg
ENST00000371953.7:c.982_983delinsAG	ENSP00000361021.3:p.Ala328Arg
ENST00000472832.2:c.409_410delinsAG	ENSP00000483066.1:p.Ala137Arg
NM_000314.5:c.982_983delinsAG	NP_000305.3:p.Ala328Arg
NM_000314.6:c.982_983delinsAG	NP_000305.3:p.Ala328Arg
NM_001304717.2:c.1501_1502delinsAG	NP_001291646.2:p.Ala501Arg
NM_001304718.1:c.391_392delinsAG	NP_001291647.1:p.Ala131Arg
XM_006717926.2:c.937_938delinsAG	XP_006717989.1:p.Ala313Arg
XM_011539981.1:c.982_983delinsAG	XP_011538283.1:p.Ala328Arg
XM_011539982.1:c.886_887delinsAG	XP_011538284.1:p.Ala296Arg
XR_945791.1:n.1552_1553delinsAG
NM_000314.7:c.982_983delinsAG	NP_000305.3:p.Ala328Arg
NM_001304717.5:c.1501_1502delinsAG	NP_001291646.4:p.Ala501Arg
NM_001304718.2:c.391_392delinsAG	NP_001291647.1:p.Ala131Arg
NM_000314.8:c.982_983delinsAG MANE Select	NP_000305.3:p.Ala328Arg