Canonical Allele Identifier: CA891835393

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87894090_87894092delinsCAA , CM000672.2:g.87894090_87894092delinsCAA	GRCh38
NC_000010.10:g.89653847_89653849delinsCAA , CM000672.1:g.89653847_89653849delinsCAA	GRCh37
NC_000010.9:g.89643827_89643829delinsCAA	NCBI36
NG_007466.2:g.35652_35654delinsCAA , LRG_311:g.35652_35654delinsCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.145_147delinsCAA	ENSP00000514759.2:p.Asn49Gln
ENST00000710265.1:c.145_147delinsCAA	ENSP00000518161.1:p.Asn49Gln
ENST00000472832.3:c.145_147delinsCAA	ENSP00000483066.2:p.Asn49Gln
ENST00000688158.2:n.899+13652_899+13654delinsCAA
ENST00000688922.2:c.145_147delinsCAA	ENSP00000508742.2:p.Asn49Gln
ENST00000700021.1:c.145_147delinsCAA	ENSP00000514757.1:p.Asn49Gln
ENST00000700022.1:c.145_147delinsCAA	ENSP00000514758.1:p.Asn49Gln
ENST00000706954.1:c.145_147delinsCAA	ENSP00000516674.1:p.Asn49Gln
ENST00000706955.1:c.*180_*182delinsCAA	ENSP00000516675.1:n.*180_*182delinsCAA
ENST00000686459.1:c.145_147delinsCAA	ENSP00000508909.1:p.Asn49Gln
ENST00000688158.1:c.*275+13652_*275+13654delinsCAA	ENSP00000509254.1:n.*275+13652_*275+13654delinsCAA
ENST00000688308.1:c.145_147delinsCAA	ENSP00000508752.1:p.Asn49Gln
ENST00000688922.1:c.14_16delinsCAA
ENST00000693560.1:c.664_666delinsCAA	ENSP00000509861.1:p.Asn222Gln
ENST00000371953.8:c.145_147delinsCAA MANE Select	ENSP00000361021.3:p.Asn49Gln
ENST00000371953.7:c.145_147delinsCAA	ENSP00000361021.3:p.Asn49Gln
ENST00000462694.1:n.147_149delinsCAA
ENST00000610634.1:c.43_45delinsCAA	ENSP00000477517.1:p.Asn15Gln
NM_000314.5:c.145_147delinsCAA	NP_000305.3:p.Asn49Gln
NM_000314.6:c.145_147delinsCAA	NP_000305.3:p.Asn49Gln
NM_001304717.2:c.664_666delinsCAA	NP_001291646.2:p.Asn222Gln
NM_001304718.1:c.-561_-559delinsCAA	NP_001291647.1:n.-561_-559delinsCAA
XM_006717926.2:c.145_147delinsCAA	XP_006717989.1:p.Asn49Gln
XM_011539981.1:c.145_147delinsCAA	XP_011538283.1:p.Asn49Gln
XM_011539982.1:c.68+13652_68+13654delinsCAA	XP_011538284.1:n.68+13652_68+13654delinsCAA
XR_945789.1:n.857_859delinsCAA
XR_945790.1:n.857_859delinsCAA
XR_945791.1:n.857_859delinsCAA
NM_000314.7:c.145_147delinsCAA	NP_000305.3:p.Asn49Gln
NM_001304717.5:c.664_666delinsCAA	NP_001291646.4:p.Asn222Gln
NM_001304718.2:c.-561_-559delinsCAA	NP_001291647.1:n.-561_-559delinsCAA
NM_000314.8:c.145_147delinsCAA MANE Select	NP_000305.3:p.Asn49Gln