Canonical Allele Identifier: CA891835079

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87894072_87894073delinsAG , CM000672.2:g.87894072_87894073delinsAG	GRCh38
NC_000010.10:g.89653829_89653830delinsAG , CM000672.1:g.89653829_89653830delinsAG	GRCh37
NC_000010.9:g.89643809_89643810delinsAG	NCBI36
NG_007466.2:g.35634_35635delinsAG , LRG_311:g.35634_35635delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.127_128delinsAG	ENSP00000514759.2:p.Glu43Arg
ENST00000710265.1:c.127_128delinsAG	ENSP00000518161.1:p.Glu43Arg
ENST00000472832.3:c.127_128delinsAG	ENSP00000483066.2:p.Glu43Arg
ENST00000688158.2:n.899+13634_899+13635delinsAG
ENST00000688922.2:c.127_128delinsAG	ENSP00000508742.2:p.Glu43Arg
ENST00000700021.1:c.127_128delinsAG	ENSP00000514757.1:p.Glu43Arg
ENST00000700022.1:c.127_128delinsAG	ENSP00000514758.1:p.Glu43Arg
ENST00000706954.1:c.127_128delinsAG	ENSP00000516674.1:p.Glu43Arg
ENST00000706955.1:c.*162_*163delinsAG	ENSP00000516675.1:n.*162_*163delinsAG
ENST00000686459.1:c.127_128delinsAG	ENSP00000508909.1:p.Glu43Arg
ENST00000688158.1:c.*275+13634_*275+13635delinsAG	ENSP00000509254.1:n.*275+13634_*275+13635delinsAG
ENST00000688308.1:c.127_128delinsAG	ENSP00000508752.1:p.Glu43Arg
ENST00000693560.1:c.646_647delinsAG	ENSP00000509861.1:p.Glu216Arg
ENST00000371953.8:c.127_128delinsAG MANE Select	ENSP00000361021.3:p.Glu43Arg
ENST00000371953.7:c.127_128delinsAG	ENSP00000361021.3:p.Glu43Arg
ENST00000462694.1:n.129_130delinsAG
ENST00000610634.1:c.25_26delinsAG	ENSP00000477517.1:p.Glu9Arg
NM_000314.5:c.127_128delinsAG	NP_000305.3:p.Glu43Arg
NM_000314.6:c.127_128delinsAG	NP_000305.3:p.Glu43Arg
NM_001304717.2:c.646_647delinsAG	NP_001291646.2:p.Glu216Arg
NM_001304718.1:c.-579_-578delinsAG	NP_001291647.1:n.-579_-578delinsAG
XM_006717926.2:c.127_128delinsAG	XP_006717989.1:p.Glu43Arg
XM_011539981.1:c.127_128delinsAG	XP_011538283.1:p.Glu43Arg
XM_011539982.1:c.68+13634_68+13635delinsAG	XP_011538284.1:n.68+13634_68+13635delinsAG
XR_945789.1:n.839_840delinsAG
XR_945790.1:n.839_840delinsAG
XR_945791.1:n.839_840delinsAG
NM_000314.7:c.127_128delinsAG	NP_000305.3:p.Glu43Arg
NM_001304717.5:c.646_647delinsAG	NP_001291646.4:p.Glu216Arg
NM_001304718.2:c.-579_-578delinsAG	NP_001291647.1:n.-579_-578delinsAG
NM_000314.8:c.127_128delinsAG MANE Select	NP_000305.3:p.Glu43Arg