Canonical Allele Identifier: CA891839592

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957910_87957911delinsAT , CM000672.2:g.87957910_87957911delinsAT	GRCh38
NC_000010.10:g.89717667_89717668delinsAT , CM000672.1:g.89717667_89717668delinsAT	GRCh37
NC_000010.9:g.89707647_89707648delinsAT	NCBI36
NG_007466.2:g.99472_99473delinsAT , LRG_311:g.99472_99473delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.692_693delinsAT	ENSP00000514759.2:p.Pro231His
ENST00000710265.1:c.692_693delinsAT	ENSP00000518161.1:p.Pro231His
ENST00000472832.3:c.692_693delinsAT	ENSP00000483066.2:p.Pro231His
ENST00000688158.2:n.1427_1428delinsAT
ENST00000688922.2:c.*522_*523delinsAT	ENSP00000508742.2:n.*522_*523delinsAT
ENST00000700021.1:c.647_648delinsAT	ENSP00000514757.1:p.Pro216His
ENST00000700022.1:c.*31_*32delinsAT	ENSP00000514758.1:n.*31_*32delinsAT
ENST00000700023.1:n.1850_1851delinsAT
ENST00000700024.1:n.2084_2085delinsAT
ENST00000700025.1:n.1461_1462delinsAT
ENST00000700026.1:n.329_330delinsAT
ENST00000700029.1:c.526_527delinsAT
ENST00000706954.1:c.692_693delinsAT	ENSP00000516674.1:p.Pro231His
ENST00000706955.1:c.*727_*728delinsAT	ENSP00000516675.1:n.*727_*728delinsAT
ENST00000686459.1:c.*278_*279delinsAT	ENSP00000508909.1:n.*278_*279delinsAT
ENST00000688158.1:c.*803_*804delinsAT	ENSP00000509254.1:n.*803_*804delinsAT
ENST00000688308.1:c.692_693delinsAT	ENSP00000508752.1:p.Pro231His
ENST00000688922.1:c.613_614delinsAT
ENST00000693560.1:c.1211_1212delinsAT	ENSP00000509861.1:p.Pro404His
ENST00000371953.8:c.692_693delinsAT MANE Select	ENSP00000361021.3:p.Pro231His
ENST00000371953.7:c.692_693delinsAT	ENSP00000361021.3:p.Pro231His
ENST00000472832.2:c.119_120delinsAT	ENSP00000483066.1:p.Pro40His
NM_000314.5:c.692_693delinsAT	NP_000305.3:p.Pro231His
NM_000314.6:c.692_693delinsAT	NP_000305.3:p.Pro231His
NM_001304717.2:c.1211_1212delinsAT	NP_001291646.2:p.Pro404His
NM_001304718.1:c.101_102delinsAT	NP_001291647.1:p.Pro34His
XM_006717926.2:c.647_648delinsAT	XP_006717989.1:p.Pro216His
XM_011539981.1:c.692_693delinsAT	XP_011538283.1:p.Pro231His
XM_011539982.1:c.596_597delinsAT	XP_011538284.1:p.Pro199His
XR_945791.1:n.1262_1263delinsAT
NM_000314.7:c.692_693delinsAT	NP_000305.3:p.Pro231His
NM_001304717.5:c.1211_1212delinsAT	NP_001291646.4:p.Pro404His
NM_001304718.2:c.101_102delinsAT	NP_001291647.1:p.Pro34His
NM_000314.8:c.692_693delinsAT MANE Select	NP_000305.3:p.Pro231His