Canonical Allele Identifier: CA891835725

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960991_87960992delinsCT , CM000672.2:g.87960991_87960992delinsCT	GRCh38
NC_000010.10:g.89720748_89720749delinsCT , CM000672.1:g.89720748_89720749delinsCT	GRCh37
NC_000010.9:g.89710728_89710729delinsCT	NCBI36
NG_007466.2:g.102553_102554delinsCT , LRG_311:g.102553_102554delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.992_993delinsCT	ENSP00000514759.2:p.Ile331Thr
ENST00000710265.1:c.899_900delinsCT	ENSP00000518161.1:p.Ile300Thr
ENST00000472832.3:c.899_900delinsCT	ENSP00000483066.2:p.Ile300Thr
ENST00000688158.2:n.1634_1635delinsCT
ENST00000688922.2:c.*729_*730delinsCT	ENSP00000508742.2:n.*729_*730delinsCT
ENST00000700021.1:c.854_855delinsCT	ENSP00000514757.1:p.Ile285Thr
ENST00000700022.1:c.*238_*239delinsCT	ENSP00000514758.1:n.*238_*239delinsCT
ENST00000700023.1:n.2057_2058delinsCT
ENST00000700024.1:n.2291_2292delinsCT
ENST00000700025.1:n.1668_1669delinsCT
ENST00000700026.1:n.536_537delinsCT
ENST00000706954.1:c.899_900delinsCT	ENSP00000516674.1:p.Ile300Thr
ENST00000706955.1:c.*934_*935delinsCT	ENSP00000516675.1:n.*934_*935delinsCT
ENST00000686459.1:c.*485_*486delinsCT	ENSP00000508909.1:n.*485_*486delinsCT
ENST00000688158.1:c.*1010_*1011delinsCT	ENSP00000509254.1:n.*1010_*1011delinsCT
ENST00000688308.1:c.899_900delinsCT	ENSP00000508752.1:p.Ile300Thr
ENST00000688922.1:c.820_821delinsCT
ENST00000693560.1:c.1418_1419delinsCT	ENSP00000509861.1:p.Ile473Thr
ENST00000371953.8:c.899_900delinsCT MANE Select	ENSP00000361021.3:p.Ile300Thr
ENST00000371953.7:c.899_900delinsCT	ENSP00000361021.3:p.Ile300Thr
ENST00000472832.2:c.326_327delinsCT	ENSP00000483066.1:p.Ile109Thr
NM_000314.5:c.899_900delinsCT	NP_000305.3:p.Ile300Thr
NM_000314.6:c.899_900delinsCT	NP_000305.3:p.Ile300Thr
NM_001304717.2:c.1418_1419delinsCT	NP_001291646.2:p.Ile473Thr
NM_001304718.1:c.308_309delinsCT	NP_001291647.1:p.Ile103Thr
XM_006717926.2:c.854_855delinsCT	XP_006717989.1:p.Ile285Thr
XM_011539981.1:c.899_900delinsCT	XP_011538283.1:p.Ile300Thr
XM_011539982.1:c.803_804delinsCT	XP_011538284.1:p.Ile268Thr
XR_945791.1:n.1469_1470delinsCT
NM_000314.7:c.899_900delinsCT	NP_000305.3:p.Ile300Thr
NM_001304717.5:c.1418_1419delinsCT	NP_001291646.4:p.Ile473Thr
NM_001304718.2:c.308_309delinsCT	NP_001291647.1:p.Ile103Thr
NM_000314.8:c.899_900delinsCT MANE Select	NP_000305.3:p.Ile300Thr