Canonical Allele Identifier: CA891834940

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960942_87960943delinsAT , CM000672.2:g.87960942_87960943delinsAT	GRCh38
NC_000010.10:g.89720699_89720700delinsAT , CM000672.1:g.89720699_89720700delinsAT	GRCh37
NC_000010.9:g.89710679_89710680delinsAT	NCBI36
NG_007466.2:g.102504_102505delinsAT , LRG_311:g.102504_102505delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.943_944delinsAT	ENSP00000514759.2:p.Glu315Met
ENST00000710265.1:c.850_851delinsAT	ENSP00000518161.1:p.Glu284Met
ENST00000472832.3:c.850_851delinsAT	ENSP00000483066.2:p.Glu284Met
ENST00000688158.2:n.1585_1586delinsAT
ENST00000688922.2:c.*680_*681delinsAT	ENSP00000508742.2:n.*680_*681delinsAT
ENST00000700021.1:c.805_806delinsAT	ENSP00000514757.1:p.Glu269Met
ENST00000700022.1:c.*189_*190delinsAT	ENSP00000514758.1:n.*189_*190delinsAT
ENST00000700023.1:n.2008_2009delinsAT
ENST00000700024.1:n.2242_2243delinsAT
ENST00000700025.1:n.1619_1620delinsAT
ENST00000700026.1:n.487_488delinsAT
ENST00000700029.1:c.777_778delinsAT
ENST00000706954.1:c.850_851delinsAT	ENSP00000516674.1:p.Glu284Met
ENST00000706955.1:c.*885_*886delinsAT	ENSP00000516675.1:n.*885_*886delinsAT
ENST00000686459.1:c.*436_*437delinsAT	ENSP00000508909.1:n.*436_*437delinsAT
ENST00000688158.1:c.*961_*962delinsAT	ENSP00000509254.1:n.*961_*962delinsAT
ENST00000688308.1:c.850_851delinsAT	ENSP00000508752.1:p.Glu284Met
ENST00000688922.1:c.771_772delinsAT
ENST00000693560.1:c.1369_1370delinsAT	ENSP00000509861.1:p.Glu457Met
ENST00000371953.8:c.850_851delinsAT MANE Select	ENSP00000361021.3:p.Glu284Met
ENST00000371953.7:c.850_851delinsAT	ENSP00000361021.3:p.Glu284Met
ENST00000472832.2:c.277_278delinsAT	ENSP00000483066.1:p.Glu93Met
NM_000314.5:c.850_851delinsAT	NP_000305.3:p.Glu284Met
NM_000314.6:c.850_851delinsAT	NP_000305.3:p.Glu284Met
NM_001304717.2:c.1369_1370delinsAT	NP_001291646.2:p.Glu457Met
NM_001304718.1:c.259_260delinsAT	NP_001291647.1:p.Glu87Met
XM_006717926.2:c.805_806delinsAT	XP_006717989.1:p.Glu269Met
XM_011539981.1:c.850_851delinsAT	XP_011538283.1:p.Glu284Met
XM_011539982.1:c.754_755delinsAT	XP_011538284.1:p.Glu252Met
XR_945791.1:n.1420_1421delinsAT
NM_000314.7:c.850_851delinsAT	NP_000305.3:p.Glu284Met
NM_001304717.5:c.1369_1370delinsAT	NP_001291646.4:p.Glu457Met
NM_001304718.2:c.259_260delinsAT	NP_001291647.1:p.Glu87Met
NM_000314.8:c.850_851delinsAT MANE Select	NP_000305.3:p.Glu284Met