Canonical Allele Identifier: CA645553934

Gene: PTEN

Linked Data

• COSMIC: COSM1167768

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957851_87957863del , CM000672.2:g.87957851_87957863del	GRCh38
NC_000010.10:g.89717608_89717620del , CM000672.1:g.89717608_89717620del	GRCh37
NC_000010.9:g.89707588_89707600del	NCBI36
NG_007466.2:g.99413_99425del , LRG_311:g.99413_99425del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.635-2_645del
ENST00000710265.1:c.635-2_645del
ENST00000472832.3:c.635-2_645del
ENST00000688158.2:n.1370-2_1380del
ENST00000688922.2:c.*465-2_*475del
ENST00000700021.1:c.590-2_600del
ENST00000700022.1:c.493-2_503del
ENST00000700023.1:n.1793-2_1803del
ENST00000700024.1:n.2027-2_2037del
ENST00000700025.1:n.1404-2_1414del
ENST00000700026.1:n.270_282del
ENST00000700029.1:c.469-2_479del
ENST00000706954.1:c.635-2_645del
ENST00000706955.1:c.*670-2_*680del
ENST00000686459.1:c.*221-2_*231del
ENST00000688158.1:c.*746-2_*756del
ENST00000688308.1:c.635-2_645del
ENST00000688922.1:c.556-2_566del
ENST00000693560.1:c.1154-2_1164del
ENST00000371953.8:c.635-2_645del
ENST00000371953.7:c.635-2_645del
ENST00000472832.2:c.62-2_72del
NM_000314.5:c.635-2_645del
NM_000314.6:c.635-2_645del
NM_001304717.2:c.1154-2_1164del
NM_001304718.1:c.44-2_54del
XM_006717926.2:c.590-2_600del
XM_011539981.1:c.635-2_645del
XM_011539982.1:c.539-2_549del
XR_945791.1:n.1205-2_1215del
NM_000314.7:c.635-2_645del
NM_001304717.5:c.1154-2_1164del
NM_001304718.2:c.44-2_54del
NM_000314.8:c.635-2_645del