Canonical Allele Identifier: CA913203394
Gene: PTEN HGNC NCBI

Linked Data

ClinVar Variation Id: 920142
dbSNP Id: rs1860548195

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957968_87957969insC , CM000672.2:g.87957968_87957969insC GRCh38
NC_000010.10:g.89717725_89717726insC , CM000672.1:g.89717725_89717726insC GRCh37
NC_000010.9:g.89707705_89707706insC NCBI36
NG_007466.2:g.99530_99531insC , LRG_311:g.99530_99531insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.750_751insC ENSP00000514759.2:p.Gly251ArgfsTer2
ENST00000710265.1:c.750_751insC ENSP00000518161.1:p.Gly251ArgfsTer2
ENST00000472832.3:c.750_751insC ENSP00000483066.2:p.Gly251ArgfsTer2
ENST00000688158.2:n.1485_1486insC
ENST00000688922.2:c.*580_*581insC ENSP00000508742.2:n.*580_*581insC
ENST00000700021.1:c.705_706insC ENSP00000514757.1:p.Gly236ArgfsTer2
ENST00000700022.1:c.*89_*90insC ENSP00000514758.1:n.*89_*90insC
ENST00000700023.1:n.1908_1909insC
ENST00000700024.1:n.2142_2143insC
ENST00000700025.1:n.1519_1520insC
ENST00000700026.1:n.387_388insC
ENST00000700029.1:c.584_585insC
ENST00000706954.1:c.750_751insC ENSP00000516674.1:p.Gly251ArgfsTer2
ENST00000706955.1:c.*785_*786insC ENSP00000516675.1:n.*785_*786insC
ENST00000686459.1:c.*336_*337insC ENSP00000508909.1:n.*336_*337insC
ENST00000688158.1:c.*861_*862insC ENSP00000509254.1:n.*861_*862insC
ENST00000688308.1:c.750_751insC ENSP00000508752.1:p.Gly251ArgfsTer2
ENST00000688922.1:c.671_672insC
ENST00000693560.1:c.1269_1270insC ENSP00000509861.1:p.Gly424ArgfsTer2
ENST00000371953.8:c.750_751insC MANE Select ENSP00000361021.3:p.Gly251ArgfsTer2
ENST00000371953.7:c.750_751insC ENSP00000361021.3:p.Gly251ArgfsTer2
ENST00000472832.2:c.177_178insC ENSP00000483066.1:p.Gly60ArgfsTer2
NM_000314.5:c.750_751insC NP_000305.3:p.Gly251ArgfsTer2
NM_000314.6:c.750_751insC NP_000305.3:p.Gly251ArgfsTer2
NM_001304717.2:c.1269_1270insC NP_001291646.2:p.Gly424ArgfsTer2
NM_001304718.1:c.159_160insC NP_001291647.1:p.Gly54ArgfsTer2
XM_006717926.2:c.705_706insC XP_006717989.1:p.Gly236ArgfsTer2
XM_011539981.1:c.750_751insC XP_011538283.1:p.Gly251ArgfsTer2
XM_011539982.1:c.654_655insC XP_011538284.1:p.Gly219ArgfsTer2
XR_945791.1:n.1320_1321insC
NM_000314.7:c.750_751insC NP_000305.3:p.Gly251ArgfsTer2
NM_001304717.5:c.1269_1270insC NP_001291646.4:p.Gly424ArgfsTer2
NM_001304718.2:c.159_160insC NP_001291647.1:p.Gly54ArgfsTer2
NM_000314.8:c.750_751insC MANE Select NP_000305.3:p.Gly251ArgfsTer2