Canonical Allele Identifier: CA891839928

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957975_87957977delinsGTT , CM000672.2:g.87957975_87957977delinsGTT	GRCh38
NC_000010.10:g.89717732_89717734delinsGTT , CM000672.1:g.89717732_89717734delinsGTT	GRCh37
NC_000010.9:g.89707712_89707714delinsGTT	NCBI36
NG_007466.2:g.99537_99539delinsGTT , LRG_311:g.99537_99539delinsGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.757_759delinsGTT	ENSP00000514759.2:p.Ile253Val
ENST00000710265.1:c.757_759delinsGTT	ENSP00000518161.1:p.Ile253Val
ENST00000472832.3:c.757_759delinsGTT	ENSP00000483066.2:p.Ile253Val
ENST00000688158.2:n.1492_1494delinsGTT
ENST00000688922.2:c.*587_*589delinsGTT	ENSP00000508742.2:n.*587_*589delinsGTT
ENST00000700021.1:c.712_714delinsGTT	ENSP00000514757.1:p.Ile238Val
ENST00000700022.1:c.*96_*98delinsGTT	ENSP00000514758.1:n.*96_*98delinsGTT
ENST00000700023.1:n.1915_1917delinsGTT
ENST00000700024.1:n.2149_2151delinsGTT
ENST00000700025.1:n.1526_1528delinsGTT
ENST00000700026.1:n.394_396delinsGTT
ENST00000700029.1:c.591_593delinsGTT
ENST00000706954.1:c.757_759delinsGTT	ENSP00000516674.1:p.Ile253Val
ENST00000706955.1:c.*792_*794delinsGTT	ENSP00000516675.1:n.*792_*794delinsGTT
ENST00000686459.1:c.*343_*345delinsGTT	ENSP00000508909.1:n.*343_*345delinsGTT
ENST00000688158.1:c.*868_*870delinsGTT	ENSP00000509254.1:n.*868_*870delinsGTT
ENST00000688308.1:c.757_759delinsGTT	ENSP00000508752.1:p.Ile253Val
ENST00000688922.1:c.678_680delinsGTT
ENST00000693560.1:c.1276_1278delinsGTT	ENSP00000509861.1:p.Ile426Val
ENST00000371953.8:c.757_759delinsGTT MANE Select	ENSP00000361021.3:p.Ile253Val
ENST00000371953.7:c.757_759delinsGTT	ENSP00000361021.3:p.Ile253Val
ENST00000472832.2:c.184_186delinsGTT	ENSP00000483066.1:p.Ile62Val
NM_000314.5:c.757_759delinsGTT	NP_000305.3:p.Ile253Val
NM_000314.6:c.757_759delinsGTT	NP_000305.3:p.Ile253Val
NM_001304717.2:c.1276_1278delinsGTT	NP_001291646.2:p.Ile426Val
NM_001304718.1:c.166_168delinsGTT	NP_001291647.1:p.Ile56Val
XM_006717926.2:c.712_714delinsGTT	XP_006717989.1:p.Ile238Val
XM_011539981.1:c.757_759delinsGTT	XP_011538283.1:p.Ile253Val
XM_011539982.1:c.661_663delinsGTT	XP_011538284.1:p.Ile221Val
XR_945791.1:n.1327_1329delinsGTT
NM_000314.7:c.757_759delinsGTT	NP_000305.3:p.Ile253Val
NM_001304717.5:c.1276_1278delinsGTT	NP_001291646.4:p.Ile426Val
NM_001304718.2:c.166_168delinsGTT	NP_001291647.1:p.Ile56Val
NM_000314.8:c.757_759delinsGTT MANE Select	NP_000305.3:p.Ile253Val