Canonical Allele Identifier: CA891834935

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960942_87960944delinsACT , CM000672.2:g.87960942_87960944delinsACT	GRCh38
NC_000010.10:g.89720699_89720701delinsACT , CM000672.1:g.89720699_89720701delinsACT	GRCh37
NC_000010.9:g.89710679_89710681delinsACT	NCBI36
NG_007466.2:g.102504_102506delinsACT , LRG_311:g.102504_102506delinsACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.943_945delinsACT	ENSP00000514759.2:p.Glu315Thr
ENST00000710265.1:c.850_852delinsACT	ENSP00000518161.1:p.Glu284Thr
ENST00000472832.3:c.850_852delinsACT	ENSP00000483066.2:p.Glu284Thr
ENST00000688158.2:n.1585_1587delinsACT
ENST00000688922.2:c.*680_*682delinsACT	ENSP00000508742.2:n.*680_*682delinsACT
ENST00000700021.1:c.805_807delinsACT	ENSP00000514757.1:p.Glu269Thr
ENST00000700022.1:c.*189_*191delinsACT	ENSP00000514758.1:n.*189_*191delinsACT
ENST00000700023.1:n.2008_2010delinsACT
ENST00000700024.1:n.2242_2244delinsACT
ENST00000700025.1:n.1619_1621delinsACT
ENST00000700026.1:n.487_489delinsACT
ENST00000700029.1:c.777_779delinsACT
ENST00000706954.1:c.850_852delinsACT	ENSP00000516674.1:p.Glu284Thr
ENST00000706955.1:c.*885_*887delinsACT	ENSP00000516675.1:n.*885_*887delinsACT
ENST00000686459.1:c.*436_*438delinsACT	ENSP00000508909.1:n.*436_*438delinsACT
ENST00000688158.1:c.*961_*963delinsACT	ENSP00000509254.1:n.*961_*963delinsACT
ENST00000688308.1:c.850_852delinsACT	ENSP00000508752.1:p.Glu284Thr
ENST00000688922.1:c.771_773delinsACT
ENST00000693560.1:c.1369_1371delinsACT	ENSP00000509861.1:p.Glu457Thr
ENST00000371953.8:c.850_852delinsACT MANE Select	ENSP00000361021.3:p.Glu284Thr
ENST00000371953.7:c.850_852delinsACT	ENSP00000361021.3:p.Glu284Thr
ENST00000472832.2:c.277_279delinsACT	ENSP00000483066.1:p.Glu93Thr
NM_000314.5:c.850_852delinsACT	NP_000305.3:p.Glu284Thr
NM_000314.6:c.850_852delinsACT	NP_000305.3:p.Glu284Thr
NM_001304717.2:c.1369_1371delinsACT	NP_001291646.2:p.Glu457Thr
NM_001304718.1:c.259_261delinsACT	NP_001291647.1:p.Glu87Thr
XM_006717926.2:c.805_807delinsACT	XP_006717989.1:p.Glu269Thr
XM_011539981.1:c.850_852delinsACT	XP_011538283.1:p.Glu284Thr
XM_011539982.1:c.754_756delinsACT	XP_011538284.1:p.Glu252Thr
XR_945791.1:n.1420_1422delinsACT
NM_000314.7:c.850_852delinsACT	NP_000305.3:p.Glu284Thr
NM_001304717.5:c.1369_1371delinsACT	NP_001291646.4:p.Glu457Thr
NM_001304718.2:c.259_261delinsACT	NP_001291647.1:p.Glu87Thr
NM_000314.8:c.850_852delinsACT MANE Select	NP_000305.3:p.Glu284Thr