Canonical Allele Identifier: CA2579926916

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952145_87952147del , CM000672.2:g.87952145_87952147del	GRCh38
NC_000010.10:g.89711902_89711904del , CM000672.1:g.89711902_89711904del	GRCh37
NC_000010.9:g.89701882_89701884del	NCBI36
NG_007466.2:g.93707_93709del , LRG_311:g.93707_93709del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.520_522del	ENSP00000514759.2:p.Tyr174del
ENST00000710265.1:c.520_522del	ENSP00000518161.1:p.Tyr174del
ENST00000472832.3:c.520_522del	ENSP00000483066.2:p.Tyr174del
ENST00000688158.2:n.1255_1257del
ENST00000688922.2:c.*350_*352del	ENSP00000508742.2:n.*350_*352del
ENST00000700021.1:c.475_477del	ENSP00000514757.1:p.Tyr159del
ENST00000700022.1:c.493-5708_493-5706del	ENSP00000514758.1:n.493-5708_493-5706del
ENST00000700023.1:n.1678_1680del
ENST00000700024.1:n.1912_1914del
ENST00000700025.1:n.1289_1291del
ENST00000700029.1:c.354_356del
ENST00000706954.1:c.520_522del	ENSP00000516674.1:p.Tyr174del
ENST00000706955.1:c.*555_*557del	ENSP00000516675.1:n.*555_*557del
ENST00000686459.1:c.*106_*108del	ENSP00000508909.1:n.*106_*108del
ENST00000688158.1:c.*631_*633del	ENSP00000509254.1:n.*631_*633del
ENST00000688308.1:c.520_522del	ENSP00000508752.1:p.Tyr174del
ENST00000688922.1:c.441_443del
ENST00000693560.1:c.1039_1041del	ENSP00000509861.1:p.Tyr347del
ENST00000371953.8:c.520_522del MANE Select	ENSP00000361021.3:p.Tyr174del
ENST00000371953.7:c.520_522del	ENSP00000361021.3:p.Tyr174del
NM_000314.5:c.520_522del	NP_000305.3:p.Tyr174del
NM_000314.6:c.520_522del	NP_000305.3:p.Tyr174del
NM_001304717.2:c.1039_1041del	NP_001291646.2:p.Tyr347del
NM_001304718.1:c.-72_-70del	NP_001291647.1:n.-72_-70del
XM_006717926.2:c.475_477del	XP_006717989.1:p.Tyr159del
XM_011539981.1:c.520_522del	XP_011538283.1:p.Tyr174del
XM_011539982.1:c.424_426del	XP_011538284.1:p.Tyr142del
XR_945789.1:n.1391_1393del
XR_945790.1:n.1508_1510del
XR_945791.1:n.1205-5708_1205-5706del
NM_000314.7:c.520_522del	NP_000305.3:p.Tyr174del
NM_001304717.5:c.1039_1041del	NP_001291646.4:p.Tyr347del
NM_001304718.2:c.-72_-70del	NP_001291647.1:n.-72_-70del
NM_000314.8:c.520_522del MANE Select	NP_000305.3:p.Tyr174del