Canonical Allele Identifier: CA891836014

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961008_87961010delinsGTT , CM000672.2:g.87961008_87961010delinsGTT	GRCh38
NC_000010.10:g.89720765_89720767delinsGTT , CM000672.1:g.89720765_89720767delinsGTT	GRCh37
NC_000010.9:g.89710745_89710747delinsGTT	NCBI36
NG_007466.2:g.102570_102572delinsGTT , LRG_311:g.102570_102572delinsGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1009_1011delinsGTT	ENSP00000514759.2:p.Ile337Val
ENST00000710265.1:c.916_918delinsGTT	ENSP00000518161.1:p.Ile306Val
ENST00000472832.3:c.916_918delinsGTT	ENSP00000483066.2:p.Ile306Val
ENST00000688158.2:n.1651_1653delinsGTT
ENST00000688922.2:c.*746_*748delinsGTT	ENSP00000508742.2:n.*746_*748delinsGTT
ENST00000700021.1:c.871_873delinsGTT	ENSP00000514757.1:p.Ile291Val
ENST00000700022.1:c.*255_*257delinsGTT	ENSP00000514758.1:n.*255_*257delinsGTT
ENST00000700023.1:n.2074_2076delinsGTT
ENST00000700024.1:n.2308_2310delinsGTT
ENST00000700025.1:n.1685_1687delinsGTT
ENST00000700026.1:n.553_555delinsGTT
ENST00000706954.1:c.916_918delinsGTT	ENSP00000516674.1:p.Ile306Val
ENST00000706955.1:c.*951_*953delinsGTT	ENSP00000516675.1:n.*951_*953delinsGTT
ENST00000686459.1:c.*502_*504delinsGTT	ENSP00000508909.1:n.*502_*504delinsGTT
ENST00000688158.1:c.*1027_*1029delinsGTT	ENSP00000509254.1:n.*1027_*1029delinsGTT
ENST00000688308.1:c.916_918delinsGTT	ENSP00000508752.1:p.Ile306Val
ENST00000688922.1:c.837_839delinsGTT
ENST00000693560.1:c.1435_1437delinsGTT	ENSP00000509861.1:p.Ile479Val
ENST00000371953.8:c.916_918delinsGTT MANE Select	ENSP00000361021.3:p.Ile306Val
ENST00000371953.7:c.916_918delinsGTT	ENSP00000361021.3:p.Ile306Val
ENST00000472832.2:c.343_345delinsGTT	ENSP00000483066.1:p.Ile115Val
NM_000314.5:c.916_918delinsGTT	NP_000305.3:p.Ile306Val
NM_000314.6:c.916_918delinsGTT	NP_000305.3:p.Ile306Val
NM_001304717.2:c.1435_1437delinsGTT	NP_001291646.2:p.Ile479Val
NM_001304718.1:c.325_327delinsGTT	NP_001291647.1:p.Ile109Val
XM_006717926.2:c.871_873delinsGTT	XP_006717989.1:p.Ile291Val
XM_011539981.1:c.916_918delinsGTT	XP_011538283.1:p.Ile306Val
XM_011539982.1:c.820_822delinsGTT	XP_011538284.1:p.Ile274Val
XR_945791.1:n.1486_1488delinsGTT
NM_000314.7:c.916_918delinsGTT	NP_000305.3:p.Ile306Val
NM_001304717.5:c.1435_1437delinsGTT	NP_001291646.4:p.Ile479Val
NM_001304718.2:c.325_327delinsGTT	NP_001291647.1:p.Ile109Val
NM_000314.8:c.916_918delinsGTT MANE Select	NP_000305.3:p.Ile306Val