Canonical Allele Identifier: CA891834813

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960933_87960935delinsTTT , CM000672.2:g.87960933_87960935delinsTTT	GRCh38
NC_000010.10:g.89720690_89720692delinsTTT , CM000672.1:g.89720690_89720692delinsTTT	GRCh37
NC_000010.9:g.89710670_89710672delinsTTT	NCBI36
NG_007466.2:g.102495_102497delinsTTT , LRG_311:g.102495_102497delinsTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.934_936delinsTTT	ENSP00000514759.2:p.Pro312Phe
ENST00000710265.1:c.841_843delinsTTT	ENSP00000518161.1:p.Pro281Phe
ENST00000472832.3:c.841_843delinsTTT	ENSP00000483066.2:p.Pro281Phe
ENST00000688158.2:n.1576_1578delinsTTT
ENST00000688922.2:c.*671_*673delinsTTT	ENSP00000508742.2:n.*671_*673delinsTTT
ENST00000700021.1:c.796_798delinsTTT	ENSP00000514757.1:p.Pro266Phe
ENST00000700022.1:c.*180_*182delinsTTT	ENSP00000514758.1:n.*180_*182delinsTTT
ENST00000700023.1:n.1999_2001delinsTTT
ENST00000700024.1:n.2233_2235delinsTTT
ENST00000700025.1:n.1610_1612delinsTTT
ENST00000700026.1:n.478_480delinsTTT
ENST00000700029.1:c.768_770delinsTTT
ENST00000706954.1:c.841_843delinsTTT	ENSP00000516674.1:p.Pro281Phe
ENST00000706955.1:c.*876_*878delinsTTT	ENSP00000516675.1:n.*876_*878delinsTTT
ENST00000686459.1:c.*427_*429delinsTTT	ENSP00000508909.1:n.*427_*429delinsTTT
ENST00000688158.1:c.*952_*954delinsTTT	ENSP00000509254.1:n.*952_*954delinsTTT
ENST00000688308.1:c.841_843delinsTTT	ENSP00000508752.1:p.Pro281Phe
ENST00000688922.1:c.762_764delinsTTT
ENST00000693560.1:c.1360_1362delinsTTT	ENSP00000509861.1:p.Pro454Phe
ENST00000371953.8:c.841_843delinsTTT MANE Select	ENSP00000361021.3:p.Pro281Phe
ENST00000371953.7:c.841_843delinsTTT	ENSP00000361021.3:p.Pro281Phe
ENST00000472832.2:c.268_270delinsTTT	ENSP00000483066.1:p.Pro90Phe
NM_000314.5:c.841_843delinsTTT	NP_000305.3:p.Pro281Phe
NM_000314.6:c.841_843delinsTTT	NP_000305.3:p.Pro281Phe
NM_001304717.2:c.1360_1362delinsTTT	NP_001291646.2:p.Pro454Phe
NM_001304718.1:c.250_252delinsTTT	NP_001291647.1:p.Pro84Phe
XM_006717926.2:c.796_798delinsTTT	XP_006717989.1:p.Pro266Phe
XM_011539981.1:c.841_843delinsTTT	XP_011538283.1:p.Pro281Phe
XM_011539982.1:c.745_747delinsTTT	XP_011538284.1:p.Pro249Phe
XR_945791.1:n.1411_1413delinsTTT
NM_000314.7:c.841_843delinsTTT	NP_000305.3:p.Pro281Phe
NM_001304717.5:c.1360_1362delinsTTT	NP_001291646.4:p.Pro454Phe
NM_001304718.2:c.250_252delinsTTT	NP_001291647.1:p.Pro84Phe
NM_000314.8:c.841_843delinsTTT MANE Select	NP_000305.3:p.Pro281Phe