Canonical Allele Identifier: CA2831650413

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87966930_87966933del , CM000672.2:g.87966930_87966933del	GRCh38
NC_000010.10:g.89726687_89726690del , CM000672.1:g.89726687_89726690del	GRCh37
NC_000010.9:g.89716667_89716670del	NCBI36
NG_007466.2:g.108492_108495del , LRG_311:g.108492_108495del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710265.1:c.*1699_*1702del	ENSP00000518161.1:n.*1699_*1702del
ENST00000688158.2:n.3405_3408del
ENST00000706954.1:c.*1458_*1461del	ENSP00000516674.1:n.*1458_*1461del
ENST00000706955.1:c.*2705_*2708del	ENSP00000516675.1:n.*2705_*2708del
ENST00000688158.1:c.*2781_*2784del	ENSP00000509254.1:n.*2781_*2784del
ENST00000693560.1:c.*1458_*1461del	ENSP00000509861.1:n.*1458_*1461del
ENST00000371953.8:c.*1458_*1461del MANE Select	ENSP00000361021.3:n.*1458_*1461del
ENST00000371953.7:c.*1458_*1461del	ENSP00000361021.3:n.*1458_*1461del
NM_000314.5:c.*1458_*1461del	NP_000305.3:n.*1458_*1461del
NM_000314.6:c.*1458_*1461del	NP_000305.3:n.*1458_*1461del
NM_001304717.2:c.*1458_*1461del	NP_001291646.2:n.*1458_*1461del
NM_001304718.1:c.*1458_*1461del	NP_001291647.1:n.*1458_*1461del
XM_006717926.2:c.*1458_*1461del	XP_006717989.1:n.*1458_*1461del
XM_011539982.1:c.*1458_*1461del	XP_011538284.1:n.*1458_*1461del
XR_945791.1:n.3240_3243del
NM_000314.7:c.*1458_*1461del	NP_000305.3:n.*1458_*1461del
NM_001304717.5:c.*1458_*1461del	NP_001291646.4:n.*1458_*1461del
NM_001304718.2:c.*1458_*1461del	NP_001291647.1:n.*1458_*1461del
NM_000314.8:c.*1458_*1461del MANE Select	NP_000305.3:n.*1458_*1461del