Canonical Allele Identifier: CA891836123

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961014_87961015delinsAA , CM000672.2:g.87961014_87961015delinsAA	GRCh38
NC_000010.10:g.89720771_89720772delinsAA , CM000672.1:g.89720771_89720772delinsAA	GRCh37
NC_000010.9:g.89710751_89710752delinsAA	NCBI36
NG_007466.2:g.102576_102577delinsAA , LRG_311:g.102576_102577delinsAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1015_1016delinsAA	ENSP00000514759.2:p.Arg339Asn
ENST00000710265.1:c.922_923delinsAA	ENSP00000518161.1:p.Arg308Asn
ENST00000472832.3:c.922_923delinsAA	ENSP00000483066.2:p.Arg308Asn
ENST00000688158.2:n.1657_1658delinsAA
ENST00000688922.2:c.*752_*753delinsAA	ENSP00000508742.2:n.*752_*753delinsAA
ENST00000700021.1:c.877_878delinsAA	ENSP00000514757.1:p.Arg293Asn
ENST00000700022.1:c.*261_*262delinsAA	ENSP00000514758.1:n.*261_*262delinsAA
ENST00000700023.1:n.2080_2081delinsAA
ENST00000700024.1:n.2314_2315delinsAA
ENST00000700025.1:n.1691_1692delinsAA
ENST00000700026.1:n.559_560delinsAA
ENST00000706954.1:c.922_923delinsAA	ENSP00000516674.1:p.Arg308Asn
ENST00000706955.1:c.*957_*958delinsAA	ENSP00000516675.1:n.*957_*958delinsAA
ENST00000686459.1:c.*508_*509delinsAA	ENSP00000508909.1:n.*508_*509delinsAA
ENST00000688158.1:c.*1033_*1034delinsAA	ENSP00000509254.1:n.*1033_*1034delinsAA
ENST00000688308.1:c.922_923delinsAA	ENSP00000508752.1:p.Arg308Asn
ENST00000688922.1:c.843_844delinsAA
ENST00000693560.1:c.1441_1442delinsAA	ENSP00000509861.1:p.Arg481Asn
ENST00000371953.8:c.922_923delinsAA MANE Select	ENSP00000361021.3:p.Arg308Asn
ENST00000371953.7:c.922_923delinsAA	ENSP00000361021.3:p.Arg308Asn
ENST00000472832.2:c.349_350delinsAA	ENSP00000483066.1:p.Arg117Asn
NM_000314.5:c.922_923delinsAA	NP_000305.3:p.Arg308Asn
NM_000314.6:c.922_923delinsAA	NP_000305.3:p.Arg308Asn
NM_001304717.2:c.1441_1442delinsAA	NP_001291646.2:p.Arg481Asn
NM_001304718.1:c.331_332delinsAA	NP_001291647.1:p.Arg111Asn
XM_006717926.2:c.877_878delinsAA	XP_006717989.1:p.Arg293Asn
XM_011539981.1:c.922_923delinsAA	XP_011538283.1:p.Arg308Asn
XM_011539982.1:c.826_827delinsAA	XP_011538284.1:p.Arg276Asn
XR_945791.1:n.1492_1493delinsAA
NM_000314.7:c.922_923delinsAA	NP_000305.3:p.Arg308Asn
NM_001304717.5:c.1441_1442delinsAA	NP_001291646.4:p.Arg481Asn
NM_001304718.2:c.331_332delinsAA	NP_001291647.1:p.Arg111Asn
NM_000314.8:c.922_923delinsAA MANE Select	NP_000305.3:p.Arg308Asn