Canonical Allele Identifier: CA645553891

Gene: PTEN

Linked Data

• COSMIC: COSM5346927

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952140_87952145del , CM000672.2:g.87952140_87952145del	GRCh38
NC_000010.10:g.89711897_89711902del , CM000672.1:g.89711897_89711902del	GRCh37
NC_000010.9:g.89701877_89701882del	NCBI36
NG_007466.2:g.93702_93707del , LRG_311:g.93702_93707del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.515_520del	ENSP00000514759.2:p.Arg172_Tyr174delinsAsn
ENST00000710265.1:c.515_520del	ENSP00000518161.1:p.Arg172_Tyr174delinsAsn
ENST00000472832.3:c.515_520del	ENSP00000483066.2:p.Arg172_Tyr174delinsAsn
ENST00000688158.2:n.1250_1255del
ENST00000688922.2:c.*345_*350del	ENSP00000508742.2:n.*345_*350del
ENST00000700021.1:c.470_475del	ENSP00000514757.1:p.Arg157_Tyr159delinsAsn
ENST00000700022.1:c.493-5713_493-5708del	ENSP00000514758.1:n.493-5713_493-5708del
ENST00000700023.1:n.1673_1678del
ENST00000700024.1:n.1907_1912del
ENST00000700025.1:n.1284_1289del
ENST00000700029.1:c.349_354del
ENST00000706954.1:c.515_520del	ENSP00000516674.1:p.Arg172_Tyr174delinsAsn
ENST00000706955.1:c.*550_*555del	ENSP00000516675.1:n.*550_*555del
ENST00000686459.1:c.*101_*106del	ENSP00000508909.1:n.*101_*106del
ENST00000688158.1:c.*626_*631del	ENSP00000509254.1:n.*626_*631del
ENST00000688308.1:c.515_520del	ENSP00000508752.1:p.Arg172_Tyr174delinsAsn
ENST00000688922.1:c.436_441del
ENST00000693560.1:c.1034_1039del	ENSP00000509861.1:p.Arg345_Tyr347delinsAsn
ENST00000371953.8:c.515_520del MANE Select	ENSP00000361021.3:p.Arg172_Tyr174delinsAsn
ENST00000371953.7:c.515_520del	ENSP00000361021.3:p.Arg172_Tyr174delinsAsn
NM_000314.5:c.515_520del	NP_000305.3:p.Arg172_Tyr174delinsAsn
NM_000314.6:c.515_520del	NP_000305.3:p.Arg172_Tyr174delinsAsn
NM_001304717.2:c.1034_1039del	NP_001291646.2:p.Arg345_Tyr347delinsAsn
NM_001304718.1:c.-77_-72del	NP_001291647.1:n.-77_-72del
XM_006717926.2:c.470_475del	XP_006717989.1:p.Arg157_Tyr159delinsAsn
XM_011539981.1:c.515_520del	XP_011538283.1:p.Arg172_Tyr174delinsAsn
XM_011539982.1:c.419_424del	XP_011538284.1:p.Arg140_Tyr142delinsAsn
XR_945789.1:n.1386_1391del
XR_945790.1:n.1503_1508del
XR_945791.1:n.1205-5713_1205-5708del
NM_000314.7:c.515_520del	NP_000305.3:p.Arg172_Tyr174delinsAsn
NM_001304717.5:c.1034_1039del	NP_001291646.4:p.Arg345_Tyr347delinsAsn
NM_001304718.2:c.-77_-72del	NP_001291647.1:n.-77_-72del
NM_000314.8:c.515_520del MANE Select	NP_000305.3:p.Arg172_Tyr174delinsAsn