Canonical Allele Identifier: CA470974072

Gene: PTEN

Linked Data

• COSMIC: COSM5751654
• MyVariant Identifiers: chr10:g.89720818_89720819insA (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961061_87961062insA , CM000672.2:g.87961061_87961062insA	GRCh38
NC_000010.10:g.89720818_89720819insA , CM000672.1:g.89720818_89720819insA	GRCh37
NC_000010.9:g.89710798_89710799insA	NCBI36
NG_007466.2:g.102623_102624insA , LRG_311:g.102623_102624insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1062_1063insA	ENSP00000514759.2:p.Asp355ArgfsTer3
ENST00000710265.1:c.969_970insA	ENSP00000518161.1:p.Asp324ArgfsTer3
ENST00000472832.3:c.969_970insA	ENSP00000483066.2:p.Asp324ArgfsTer3
ENST00000688158.2:n.1704_1705insA
ENST00000688922.2:c.*799_*800insA	ENSP00000508742.2:n.*799_*800insA
ENST00000700021.1:c.924_925insA	ENSP00000514757.1:p.Asp309ArgfsTer3
ENST00000700022.1:c.*308_*309insA	ENSP00000514758.1:n.*308_*309insA
ENST00000700023.1:n.2127_2128insA
ENST00000700024.1:n.2361_2362insA
ENST00000700025.1:n.1738_1739insA
ENST00000700026.1:n.606_607insA
ENST00000706954.1:c.969_970insA	ENSP00000516674.1:p.Asp324ArgfsTer3
ENST00000706955.1:c.*1004_*1005insA	ENSP00000516675.1:n.*1004_*1005insA
ENST00000686459.1:c.*555_*556insA	ENSP00000508909.1:n.*555_*556insA
ENST00000688158.1:c.*1080_*1081insA	ENSP00000509254.1:n.*1080_*1081insA
ENST00000688308.1:c.969_970insA	ENSP00000508752.1:p.Asp324ArgfsTer3
ENST00000688922.1:c.890_891insA
ENST00000693560.1:c.1488_1489insA	ENSP00000509861.1:p.Asp497ArgfsTer3
ENST00000371953.8:c.969_970insA MANE Select	ENSP00000361021.3:p.Asp324ArgfsTer3
ENST00000371953.7:c.969_970insA	ENSP00000361021.3:p.Asp324ArgfsTer3
ENST00000472832.2:c.396_397insA	ENSP00000483066.1:p.Asp133ArgfsTer3
NM_000314.5:c.969_970insA	NP_000305.3:p.Asp324ArgfsTer3
NM_000314.6:c.969_970insA	NP_000305.3:p.Asp324ArgfsTer3
NM_001304717.2:c.1488_1489insA	NP_001291646.2:p.Asp497ArgfsTer3
NM_001304718.1:c.378_379insA	NP_001291647.1:p.Asp127ArgfsTer3
XM_006717926.2:c.924_925insA	XP_006717989.1:p.Asp309ArgfsTer3
XM_011539981.1:c.969_970insA	XP_011538283.1:p.Asp324ArgfsTer3
XM_011539982.1:c.873_874insA	XP_011538284.1:p.Asp292ArgfsTer3
XR_945791.1:n.1539_1540insA
NM_000314.7:c.969_970insA	NP_000305.3:p.Asp324ArgfsTer3
NM_001304717.5:c.1488_1489insA	NP_001291646.4:p.Asp497ArgfsTer3
NM_001304718.2:c.378_379insA	NP_001291647.1:p.Asp127ArgfsTer3
NM_000314.8:c.969_970insA MANE Select	NP_000305.3:p.Asp324ArgfsTer3