Canonical Allele Identifier: CA1926176075

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87967011_87967012delinsAT , CM000672.2:g.87967011_87967012delinsAT	GRCh38
NC_000010.10:g.89726768_89726769delinsAT , CM000672.1:g.89726768_89726769delinsAT	GRCh37
NC_000010.9:g.89716748_89716749delinsAT	NCBI36
NG_007466.2:g.108573_108574delinsAT , LRG_311:g.108573_108574delinsAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000710265.1:c.*1780_*1781delinsAT	ENSP00000518161.1:n.*1780_*1781delinsAT
ENST00000688158.2:n.3486_3487delinsAT
ENST00000706954.1:c.*1539_*1540delinsAT	ENSP00000516674.1:n.*1539_*1540delinsAT
ENST00000706955.1:c.*2786_*2787delinsAT	ENSP00000516675.1:n.*2786_*2787delinsAT
ENST00000688158.1:c.*2862_*2863delinsAT	ENSP00000509254.1:n.*2862_*2863delinsAT
ENST00000693560.1:c.*1539_*1540delinsAT	ENSP00000509861.1:n.*1539_*1540delinsAT
ENST00000371953.8:c.*1539_*1540delinsAT MANE Select	ENSP00000361021.3:n.*1539_*1540delinsAT
ENST00000371953.7:c.*1539_*1540delinsAT	ENSP00000361021.3:n.*1539_*1540delinsAT
NM_000314.5:c.*1539_*1540delinsAT	NP_000305.3:n.*1539_*1540delinsAT
NM_000314.6:c.*1539_*1540delinsAT	NP_000305.3:n.*1539_*1540delinsAT
NM_001304717.2:c.*1539_*1540delinsAT	NP_001291646.2:n.*1539_*1540delinsAT
NM_001304718.1:c.*1539_*1540delinsAT	NP_001291647.1:n.*1539_*1540delinsAT
XM_006717926.2:c.*1539_*1540delinsAT	XP_006717989.1:n.*1539_*1540delinsAT
XM_011539982.1:c.*1539_*1540delinsAT	XP_011538284.1:n.*1539_*1540delinsAT
XR_945791.1:n.3321_3322delinsAT
NM_000314.7:c.*1539_*1540delinsAT	NP_000305.3:n.*1539_*1540delinsAT
NM_001304717.5:c.*1539_*1540delinsAT	NP_001291646.4:n.*1539_*1540delinsAT
NM_001304718.2:c.*1539_*1540delinsAT	NP_001291647.1:n.*1539_*1540delinsAT
NM_000314.8:c.*1539_*1540delinsAT MANE Select	NP_000305.3:n.*1539_*1540delinsAT