Canonical Allele Identifier: CA891838806

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952158_87952159delinsGG , CM000672.2:g.87952158_87952159delinsGG	GRCh38
NC_000010.10:g.89711915_89711916delinsGG , CM000672.1:g.89711915_89711916delinsGG	GRCh37
NC_000010.9:g.89701895_89701896delinsGG	NCBI36
NG_007466.2:g.93720_93721delinsGG , LRG_311:g.93720_93721delinsGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.533_534delinsGG	ENSP00000514759.2:p.Tyr178Trp
ENST00000710265.1:c.533_534delinsGG	ENSP00000518161.1:p.Tyr178Trp
ENST00000472832.3:c.533_534delinsGG	ENSP00000483066.2:p.Tyr178Trp
ENST00000688158.2:n.1268_1269delinsGG
ENST00000688922.2:c.*363_*364delinsGG	ENSP00000508742.2:n.*363_*364delinsGG
ENST00000700021.1:c.488_489delinsGG	ENSP00000514757.1:p.Tyr163Trp
ENST00000700022.1:c.493-5695_493-5694delinsGG	ENSP00000514758.1:n.493-5695_493-5694deli...
ENST00000700023.1:n.1691_1692delinsGG
ENST00000700024.1:n.1925_1926delinsGG
ENST00000700025.1:n.1302_1303delinsGG
ENST00000700029.1:c.367_368delinsGG
ENST00000706954.1:c.533_534delinsGG	ENSP00000516674.1:p.Tyr178Trp
ENST00000706955.1:c.*568_*569delinsGG	ENSP00000516675.1:n.*568_*569delinsGG
ENST00000686459.1:c.*119_*120delinsGG	ENSP00000508909.1:n.*119_*120delinsGG
ENST00000688158.1:c.*644_*645delinsGG	ENSP00000509254.1:n.*644_*645delinsGG
ENST00000688308.1:c.533_534delinsGG	ENSP00000508752.1:p.Tyr178Trp
ENST00000688922.1:c.454_455delinsGG
ENST00000693560.1:c.1052_1053delinsGG	ENSP00000509861.1:p.Tyr351Trp
ENST00000371953.8:c.533_534delinsGG MANE Select	ENSP00000361021.3:p.Tyr178Trp
ENST00000371953.7:c.533_534delinsGG	ENSP00000361021.3:p.Tyr178Trp
NM_000314.5:c.533_534delinsGG	NP_000305.3:p.Tyr178Trp
NM_000314.6:c.533_534delinsGG	NP_000305.3:p.Tyr178Trp
NM_001304717.2:c.1052_1053delinsGG	NP_001291646.2:p.Tyr351Trp
NM_001304718.1:c.-59_-58delinsGG	NP_001291647.1:n.-59_-58delinsGG
XM_006717926.2:c.488_489delinsGG	XP_006717989.1:p.Tyr163Trp
XM_011539981.1:c.533_534delinsGG	XP_011538283.1:p.Tyr178Trp
XM_011539982.1:c.437_438delinsGG	XP_011538284.1:p.Tyr146Trp
XR_945789.1:n.1404_1405delinsGG
XR_945790.1:n.1521_1522delinsGG
XR_945791.1:n.1205-5695_1205-5694delinsGG
NM_000314.7:c.533_534delinsGG	NP_000305.3:p.Tyr178Trp
NM_001304717.5:c.1052_1053delinsGG	NP_001291646.4:p.Tyr351Trp
NM_001304718.2:c.-59_-58delinsGG	NP_001291647.1:n.-59_-58delinsGG
NM_000314.8:c.533_534delinsGG MANE Select	NP_000305.3:p.Tyr178Trp