Canonical Allele Identifier: CA1926188586
Gene: PTEN HGNC NCBI

Linked Data

ClinVar Variation Id: 1047317
ClinVar RCV Id: RCV001352012
dbSNP Id: rs1860548195

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957968_87957969insCAC , CM000672.2:g.87957968_87957969insCAC GRCh38
NC_000010.10:g.89717725_89717726insCAC , CM000672.1:g.89717725_89717726insCAC GRCh37
NC_000010.9:g.89707705_89707706insCAC NCBI36
NG_007466.2:g.99530_99531insCAC , LRG_311:g.99530_99531insCAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.750_751insCAC ENSP00000514759.2:p.Cys250_Gly251insHis
ENST00000710265.1:c.750_751insCAC ENSP00000518161.1:p.Cys250_Gly251insHis
ENST00000472832.3:c.750_751insCAC ENSP00000483066.2:p.Cys250_Gly251insHis
ENST00000688158.2:n.1485_1486insCAC
ENST00000688922.2:c.*580_*581insCAC ENSP00000508742.2:n.*580_*581insCAC
ENST00000700021.1:c.705_706insCAC ENSP00000514757.1:p.Cys235_Gly236insHis
ENST00000700022.1:c.*89_*90insCAC ENSP00000514758.1:n.*89_*90insCAC
ENST00000700023.1:n.1908_1909insCAC
ENST00000700024.1:n.2142_2143insCAC
ENST00000700025.1:n.1519_1520insCAC
ENST00000700026.1:n.387_388insCAC
ENST00000700029.1:c.584_585insCAC
ENST00000706954.1:c.750_751insCAC ENSP00000516674.1:p.Cys250_Gly251insHis
ENST00000706955.1:c.*785_*786insCAC ENSP00000516675.1:n.*785_*786insCAC
ENST00000686459.1:c.*336_*337insCAC ENSP00000508909.1:n.*336_*337insCAC
ENST00000688158.1:c.*861_*862insCAC ENSP00000509254.1:n.*861_*862insCAC
ENST00000688308.1:c.750_751insCAC ENSP00000508752.1:p.Cys250_Gly251insHis
ENST00000688922.1:c.671_672insCAC
ENST00000693560.1:c.1269_1270insCAC ENSP00000509861.1:p.Cys423_Gly424insHis
ENST00000371953.8:c.750_751insCAC MANE Select ENSP00000361021.3:p.Cys250_Gly251insHis
ENST00000371953.7:c.750_751insCAC ENSP00000361021.3:p.Cys250_Gly251insHis
ENST00000472832.2:c.177_178insCAC ENSP00000483066.1:p.Cys59_Gly60insHis
NM_000314.5:c.750_751insCAC NP_000305.3:p.Cys250_Gly251insHis
NM_000314.6:c.750_751insCAC NP_000305.3:p.Cys250_Gly251insHis
NM_001304717.2:c.1269_1270insCAC NP_001291646.2:p.Cys423_Gly424insHis
NM_001304718.1:c.159_160insCAC NP_001291647.1:p.Cys53_Gly54insHis
XM_006717926.2:c.705_706insCAC XP_006717989.1:p.Cys235_Gly236insHis
XM_011539981.1:c.750_751insCAC XP_011538283.1:p.Cys250_Gly251insHis
XM_011539982.1:c.654_655insCAC XP_011538284.1:p.Cys218_Gly219insHis
XR_945791.1:n.1320_1321insCAC
NM_000314.7:c.750_751insCAC NP_000305.3:p.Cys250_Gly251insHis
NM_001304717.5:c.1269_1270insCAC NP_001291646.4:p.Cys423_Gly424insHis
NM_001304718.2:c.159_160insCAC NP_001291647.1:p.Cys53_Gly54insHis
NM_000314.8:c.750_751insCAC MANE Select NP_000305.3:p.Cys250_Gly251insHis