Canonical Allele Identifier: CA891838750

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952145_87952146delinsAT , CM000672.2:g.87952145_87952146delinsAT	GRCh38
NC_000010.10:g.89711902_89711903delinsAT , CM000672.1:g.89711902_89711903delinsAT	GRCh37
NC_000010.9:g.89701882_89701883delinsAT	NCBI36
NG_007466.2:g.93707_93708delinsAT , LRG_311:g.93707_93708delinsAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.520_521delinsAT	ENSP00000514759.2:p.Tyr174Ile
ENST00000710265.1:c.520_521delinsAT	ENSP00000518161.1:p.Tyr174Ile
ENST00000472832.3:c.520_521delinsAT	ENSP00000483066.2:p.Tyr174Ile
ENST00000688158.2:n.1255_1256delinsAT
ENST00000688922.2:c.*350_*351delinsAT	ENSP00000508742.2:n.*350_*351delinsAT
ENST00000700021.1:c.475_476delinsAT	ENSP00000514757.1:p.Tyr159Ile
ENST00000700022.1:c.493-5708_493-5707delinsAT	ENSP00000514758.1:n.493-5708_493-5707deli...
ENST00000700023.1:n.1678_1679delinsAT
ENST00000700024.1:n.1912_1913delinsAT
ENST00000700025.1:n.1289_1290delinsAT
ENST00000700029.1:c.354_355delinsAT
ENST00000706954.1:c.520_521delinsAT	ENSP00000516674.1:p.Tyr174Ile
ENST00000706955.1:c.*555_*556delinsAT	ENSP00000516675.1:n.*555_*556delinsAT
ENST00000686459.1:c.*106_*107delinsAT	ENSP00000508909.1:n.*106_*107delinsAT
ENST00000688158.1:c.*631_*632delinsAT	ENSP00000509254.1:n.*631_*632delinsAT
ENST00000688308.1:c.520_521delinsAT	ENSP00000508752.1:p.Tyr174Ile
ENST00000688922.1:c.441_442delinsAT
ENST00000693560.1:c.1039_1040delinsAT	ENSP00000509861.1:p.Tyr347Ile
ENST00000371953.8:c.520_521delinsAT MANE Select	ENSP00000361021.3:p.Tyr174Ile
ENST00000371953.7:c.520_521delinsAT	ENSP00000361021.3:p.Tyr174Ile
NM_000314.5:c.520_521delinsAT	NP_000305.3:p.Tyr174Ile
NM_000314.6:c.520_521delinsAT	NP_000305.3:p.Tyr174Ile
NM_001304717.2:c.1039_1040delinsAT	NP_001291646.2:p.Tyr347Ile
NM_001304718.1:c.-72_-71delinsAT	NP_001291647.1:n.-72_-71delinsAT
XM_006717926.2:c.475_476delinsAT	XP_006717989.1:p.Tyr159Ile
XM_011539981.1:c.520_521delinsAT	XP_011538283.1:p.Tyr174Ile
XM_011539982.1:c.424_425delinsAT	XP_011538284.1:p.Tyr142Ile
XR_945789.1:n.1391_1392delinsAT
XR_945790.1:n.1508_1509delinsAT
XR_945791.1:n.1205-5708_1205-5707delinsAT
NM_000314.7:c.520_521delinsAT	NP_000305.3:p.Tyr174Ile
NM_001304717.5:c.1039_1040delinsAT	NP_001291646.4:p.Tyr347Ile
NM_001304718.2:c.-72_-71delinsAT	NP_001291647.1:n.-72_-71delinsAT
NM_000314.8:c.520_521delinsAT MANE Select	NP_000305.3:p.Tyr174Ile