Canonical Allele Identifier: CA891834814

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960933_87960935delinsTAT , CM000672.2:g.87960933_87960935delinsTAT	GRCh38
NC_000010.10:g.89720690_89720692delinsTAT , CM000672.1:g.89720690_89720692delinsTAT	GRCh37
NC_000010.9:g.89710670_89710672delinsTAT	NCBI36
NG_007466.2:g.102495_102497delinsTAT , LRG_311:g.102495_102497delinsTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.934_936delinsTAT	ENSP00000514759.2:p.Pro312Tyr
ENST00000710265.1:c.841_843delinsTAT	ENSP00000518161.1:p.Pro281Tyr
ENST00000472832.3:c.841_843delinsTAT	ENSP00000483066.2:p.Pro281Tyr
ENST00000688158.2:n.1576_1578delinsTAT
ENST00000688922.2:c.*671_*673delinsTAT	ENSP00000508742.2:n.*671_*673delinsTAT
ENST00000700021.1:c.796_798delinsTAT	ENSP00000514757.1:p.Pro266Tyr
ENST00000700022.1:c.*180_*182delinsTAT	ENSP00000514758.1:n.*180_*182delinsTAT
ENST00000700023.1:n.1999_2001delinsTAT
ENST00000700024.1:n.2233_2235delinsTAT
ENST00000700025.1:n.1610_1612delinsTAT
ENST00000700026.1:n.478_480delinsTAT
ENST00000700029.1:c.768_770delinsTAT
ENST00000706954.1:c.841_843delinsTAT	ENSP00000516674.1:p.Pro281Tyr
ENST00000706955.1:c.*876_*878delinsTAT	ENSP00000516675.1:n.*876_*878delinsTAT
ENST00000686459.1:c.*427_*429delinsTAT	ENSP00000508909.1:n.*427_*429delinsTAT
ENST00000688158.1:c.*952_*954delinsTAT	ENSP00000509254.1:n.*952_*954delinsTAT
ENST00000688308.1:c.841_843delinsTAT	ENSP00000508752.1:p.Pro281Tyr
ENST00000688922.1:c.762_764delinsTAT
ENST00000693560.1:c.1360_1362delinsTAT	ENSP00000509861.1:p.Pro454Tyr
ENST00000371953.8:c.841_843delinsTAT MANE Select	ENSP00000361021.3:p.Pro281Tyr
ENST00000371953.7:c.841_843delinsTAT	ENSP00000361021.3:p.Pro281Tyr
ENST00000472832.2:c.268_270delinsTAT	ENSP00000483066.1:p.Pro90Tyr
NM_000314.5:c.841_843delinsTAT	NP_000305.3:p.Pro281Tyr
NM_000314.6:c.841_843delinsTAT	NP_000305.3:p.Pro281Tyr
NM_001304717.2:c.1360_1362delinsTAT	NP_001291646.2:p.Pro454Tyr
NM_001304718.1:c.250_252delinsTAT	NP_001291647.1:p.Pro84Tyr
XM_006717926.2:c.796_798delinsTAT	XP_006717989.1:p.Pro266Tyr
XM_011539981.1:c.841_843delinsTAT	XP_011538283.1:p.Pro281Tyr
XM_011539982.1:c.745_747delinsTAT	XP_011538284.1:p.Pro249Tyr
XR_945791.1:n.1411_1413delinsTAT
NM_000314.7:c.841_843delinsTAT	NP_000305.3:p.Pro281Tyr
NM_001304717.5:c.1360_1362delinsTAT	NP_001291646.4:p.Pro454Tyr
NM_001304718.2:c.250_252delinsTAT	NP_001291647.1:p.Pro84Tyr
NM_000314.8:c.841_843delinsTAT MANE Select	NP_000305.3:p.Pro281Tyr