Canonical Allele Identifier: CA891838753

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952145_87952146delinsGC , CM000672.2:g.87952145_87952146delinsGC	GRCh38
NC_000010.10:g.89711902_89711903delinsGC , CM000672.1:g.89711902_89711903delinsGC	GRCh37
NC_000010.9:g.89701882_89701883delinsGC	NCBI36
NG_007466.2:g.93707_93708delinsGC , LRG_311:g.93707_93708delinsGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.520_521delinsGC	ENSP00000514759.2:p.Tyr174Ala
ENST00000710265.1:c.520_521delinsGC	ENSP00000518161.1:p.Tyr174Ala
ENST00000472832.3:c.520_521delinsGC	ENSP00000483066.2:p.Tyr174Ala
ENST00000688158.2:n.1255_1256delinsGC
ENST00000688922.2:c.*350_*351delinsGC	ENSP00000508742.2:n.*350_*351delinsGC
ENST00000700021.1:c.475_476delinsGC	ENSP00000514757.1:p.Tyr159Ala
ENST00000700022.1:c.493-5708_493-5707delinsGC	ENSP00000514758.1:n.493-5708_493-5707deli...
ENST00000700023.1:n.1678_1679delinsGC
ENST00000700024.1:n.1912_1913delinsGC
ENST00000700025.1:n.1289_1290delinsGC
ENST00000700029.1:c.354_355delinsGC
ENST00000706954.1:c.520_521delinsGC	ENSP00000516674.1:p.Tyr174Ala
ENST00000706955.1:c.*555_*556delinsGC	ENSP00000516675.1:n.*555_*556delinsGC
ENST00000686459.1:c.*106_*107delinsGC	ENSP00000508909.1:n.*106_*107delinsGC
ENST00000688158.1:c.*631_*632delinsGC	ENSP00000509254.1:n.*631_*632delinsGC
ENST00000688308.1:c.520_521delinsGC	ENSP00000508752.1:p.Tyr174Ala
ENST00000688922.1:c.441_442delinsGC
ENST00000693560.1:c.1039_1040delinsGC	ENSP00000509861.1:p.Tyr347Ala
ENST00000371953.8:c.520_521delinsGC MANE Select	ENSP00000361021.3:p.Tyr174Ala
ENST00000371953.7:c.520_521delinsGC	ENSP00000361021.3:p.Tyr174Ala
NM_000314.5:c.520_521delinsGC	NP_000305.3:p.Tyr174Ala
NM_000314.6:c.520_521delinsGC	NP_000305.3:p.Tyr174Ala
NM_001304717.2:c.1039_1040delinsGC	NP_001291646.2:p.Tyr347Ala
NM_001304718.1:c.-72_-71delinsGC	NP_001291647.1:n.-72_-71delinsGC
XM_006717926.2:c.475_476delinsGC	XP_006717989.1:p.Tyr159Ala
XM_011539981.1:c.520_521delinsGC	XP_011538283.1:p.Tyr174Ala
XM_011539982.1:c.424_425delinsGC	XP_011538284.1:p.Tyr142Ala
XR_945789.1:n.1391_1392delinsGC
XR_945790.1:n.1508_1509delinsGC
XR_945791.1:n.1205-5708_1205-5707delinsGC
NM_000314.7:c.520_521delinsGC	NP_000305.3:p.Tyr174Ala
NM_001304717.5:c.1039_1040delinsGC	NP_001291646.4:p.Tyr347Ala
NM_001304718.2:c.-72_-71delinsGC	NP_001291647.1:n.-72_-71delinsGC
NM_000314.8:c.520_521delinsGC MANE Select	NP_000305.3:p.Tyr174Ala