Canonical Allele Identifier: CA891839585

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957909_87957911delinsGTT , CM000672.2:g.87957909_87957911delinsGTT	GRCh38
NC_000010.10:g.89717666_89717668delinsGTT , CM000672.1:g.89717666_89717668delinsGTT	GRCh37
NC_000010.9:g.89707646_89707648delinsGTT	NCBI36
NG_007466.2:g.99471_99473delinsGTT , LRG_311:g.99471_99473delinsGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.691_693delinsGTT	ENSP00000514759.2:p.Pro231Val
ENST00000710265.1:c.691_693delinsGTT	ENSP00000518161.1:p.Pro231Val
ENST00000472832.3:c.691_693delinsGTT	ENSP00000483066.2:p.Pro231Val
ENST00000688158.2:n.1426_1428delinsGTT
ENST00000688922.2:c.*521_*523delinsGTT	ENSP00000508742.2:n.*521_*523delinsGTT
ENST00000700021.1:c.646_648delinsGTT	ENSP00000514757.1:p.Pro216Val
ENST00000700022.1:c.*30_*32delinsGTT	ENSP00000514758.1:n.*30_*32delinsGTT
ENST00000700023.1:n.1849_1851delinsGTT
ENST00000700024.1:n.2083_2085delinsGTT
ENST00000700025.1:n.1460_1462delinsGTT
ENST00000700026.1:n.328_330delinsGTT
ENST00000700029.1:c.525_527delinsGTT
ENST00000706954.1:c.691_693delinsGTT	ENSP00000516674.1:p.Pro231Val
ENST00000706955.1:c.*726_*728delinsGTT	ENSP00000516675.1:n.*726_*728delinsGTT
ENST00000686459.1:c.*277_*279delinsGTT	ENSP00000508909.1:n.*277_*279delinsGTT
ENST00000688158.1:c.*802_*804delinsGTT	ENSP00000509254.1:n.*802_*804delinsGTT
ENST00000688308.1:c.691_693delinsGTT	ENSP00000508752.1:p.Pro231Val
ENST00000688922.1:c.612_614delinsGTT
ENST00000693560.1:c.1210_1212delinsGTT	ENSP00000509861.1:p.Pro404Val
ENST00000371953.8:c.691_693delinsGTT MANE Select	ENSP00000361021.3:p.Pro231Val
ENST00000371953.7:c.691_693delinsGTT	ENSP00000361021.3:p.Pro231Val
ENST00000472832.2:c.118_120delinsGTT	ENSP00000483066.1:p.Pro40Val
NM_000314.5:c.691_693delinsGTT	NP_000305.3:p.Pro231Val
NM_000314.6:c.691_693delinsGTT	NP_000305.3:p.Pro231Val
NM_001304717.2:c.1210_1212delinsGTT	NP_001291646.2:p.Pro404Val
NM_001304718.1:c.100_102delinsGTT	NP_001291647.1:p.Pro34Val
XM_006717926.2:c.646_648delinsGTT	XP_006717989.1:p.Pro216Val
XM_011539981.1:c.691_693delinsGTT	XP_011538283.1:p.Pro231Val
XM_011539982.1:c.595_597delinsGTT	XP_011538284.1:p.Pro199Val
XR_945791.1:n.1261_1263delinsGTT
NM_000314.7:c.691_693delinsGTT	NP_000305.3:p.Pro231Val
NM_001304717.5:c.1210_1212delinsGTT	NP_001291646.4:p.Pro404Val
NM_001304718.2:c.100_102delinsGTT	NP_001291647.1:p.Pro34Val
NM_000314.8:c.691_693delinsGTT MANE Select	NP_000305.3:p.Pro231Val