Canonical Allele Identifier: CA891839591

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957910_87957911delinsAA , CM000672.2:g.87957910_87957911delinsAA	GRCh38
NC_000010.10:g.89717667_89717668delinsAA , CM000672.1:g.89717667_89717668delinsAA	GRCh37
NC_000010.9:g.89707647_89707648delinsAA	NCBI36
NG_007466.2:g.99472_99473delinsAA , LRG_311:g.99472_99473delinsAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.692_693delinsAA	ENSP00000514759.2:p.Pro231Gln
ENST00000710265.1:c.692_693delinsAA	ENSP00000518161.1:p.Pro231Gln
ENST00000472832.3:c.692_693delinsAA	ENSP00000483066.2:p.Pro231Gln
ENST00000688158.2:n.1427_1428delinsAA
ENST00000688922.2:c.*522_*523delinsAA	ENSP00000508742.2:n.*522_*523delinsAA
ENST00000700021.1:c.647_648delinsAA	ENSP00000514757.1:p.Pro216Gln
ENST00000700022.1:c.*31_*32delinsAA	ENSP00000514758.1:n.*31_*32delinsAA
ENST00000700023.1:n.1850_1851delinsAA
ENST00000700024.1:n.2084_2085delinsAA
ENST00000700025.1:n.1461_1462delinsAA
ENST00000700026.1:n.329_330delinsAA
ENST00000700029.1:c.526_527delinsAA
ENST00000706954.1:c.692_693delinsAA	ENSP00000516674.1:p.Pro231Gln
ENST00000706955.1:c.*727_*728delinsAA	ENSP00000516675.1:n.*727_*728delinsAA
ENST00000686459.1:c.*278_*279delinsAA	ENSP00000508909.1:n.*278_*279delinsAA
ENST00000688158.1:c.*803_*804delinsAA	ENSP00000509254.1:n.*803_*804delinsAA
ENST00000688308.1:c.692_693delinsAA	ENSP00000508752.1:p.Pro231Gln
ENST00000688922.1:c.613_614delinsAA
ENST00000693560.1:c.1211_1212delinsAA	ENSP00000509861.1:p.Pro404Gln
ENST00000371953.8:c.692_693delinsAA MANE Select	ENSP00000361021.3:p.Pro231Gln
ENST00000371953.7:c.692_693delinsAA	ENSP00000361021.3:p.Pro231Gln
ENST00000472832.2:c.119_120delinsAA	ENSP00000483066.1:p.Pro40Gln
NM_000314.5:c.692_693delinsAA	NP_000305.3:p.Pro231Gln
NM_000314.6:c.692_693delinsAA	NP_000305.3:p.Pro231Gln
NM_001304717.2:c.1211_1212delinsAA	NP_001291646.2:p.Pro404Gln
NM_001304718.1:c.101_102delinsAA	NP_001291647.1:p.Pro34Gln
XM_006717926.2:c.647_648delinsAA	XP_006717989.1:p.Pro216Gln
XM_011539981.1:c.692_693delinsAA	XP_011538283.1:p.Pro231Gln
XM_011539982.1:c.596_597delinsAA	XP_011538284.1:p.Pro199Gln
XR_945791.1:n.1262_1263delinsAA
NM_000314.7:c.692_693delinsAA	NP_000305.3:p.Pro231Gln
NM_001304717.5:c.1211_1212delinsAA	NP_001291646.4:p.Pro404Gln
NM_001304718.2:c.101_102delinsAA	NP_001291647.1:p.Pro34Gln
NM_000314.8:c.692_693delinsAA MANE Select	NP_000305.3:p.Pro231Gln