Canonical Allele Identifier: CA1926188640
Gene: PTEN HGNC NCBI

Linked Data

dbSNP Id: rs1860553112
gnomAD v4: 10-87958029-T-TG
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87958029_87958030insG , CM000672.2:g.87958029_87958030insG GRCh38
NC_000010.10:g.89717786_89717787insG , CM000672.1:g.89717786_89717787insG GRCh37
NC_000010.9:g.89707766_89707767insG NCBI36
NG_007466.2:g.99591_99592insG , LRG_311:g.99591_99592insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.801+10_801+11insG ENSP00000514759.2:n.801+10_801+11insG
ENST00000710265.1:c.801+10_801+11insG ENSP00000518161.1:n.801+10_801+11insG
ENST00000472832.3:c.801+10_801+11insG ENSP00000483066.2:n.801+10_801+11insG
ENST00000688158.2:n.1536+10_1536+11insG
ENST00000688922.2:c.*631+10_*631+11insG ENSP00000508742.2:n.*631+10_*631+11insG
ENST00000700021.1:c.756+10_756+11insG ENSP00000514757.1:n.756+10_756+11insG
ENST00000700022.1:c.*140+10_*140+11insG ENSP00000514758.1:n.*140+10_*140+11insG
ENST00000700023.1:n.1959+10_1959+11insG
ENST00000700024.1:n.2193+10_2193+11insG
ENST00000700025.1:n.1570+10_1570+11insG
ENST00000700026.1:n.438+10_438+11insG
ENST00000700029.1:c.635+10_635+11insG
ENST00000706954.1:c.801+10_801+11insG ENSP00000516674.1:n.801+10_801+11insG
ENST00000706955.1:c.*836+10_*836+11insG ENSP00000516675.1:n.*836+10_*836+11insG
ENST00000686459.1:c.*387+10_*387+11insG ENSP00000508909.1:n.*387+10_*387+11insG
ENST00000688158.1:c.*912+10_*912+11insG ENSP00000509254.1:n.*912+10_*912+11insG
ENST00000688308.1:c.801+10_801+11insG ENSP00000508752.1:n.801+10_801+11insG
ENST00000688922.1:c.722+10_722+11insG
ENST00000693560.1:c.1320+10_1320+11insG ENSP00000509861.1:n.1320+10_1320+11insG
ENST00000371953.8:c.801+10_801+11insG MANE Select ENSP00000361021.3:n.801+10_801+11insG
ENST00000371953.7:c.801+10_801+11insG ENSP00000361021.3:n.801+10_801+11insG
ENST00000472832.2:c.228+10_228+11insG ENSP00000483066.1:n.228+10_228+11insG
NM_000314.5:c.801+10_801+11insG NP_000305.3:n.801+10_801+11insG
NM_000314.6:c.801+10_801+11insG NP_000305.3:n.801+10_801+11insG
NM_001304717.2:c.1320+10_1320+11insG NP_001291646.2:n.1320+10_1320+11insG
NM_001304718.1:c.210+10_210+11insG NP_001291647.1:n.210+10_210+11insG
XM_006717926.2:c.756+10_756+11insG XP_006717989.1:n.756+10_756+11insG
XM_011539981.1:c.801+10_801+11insG XP_011538283.1:n.801+10_801+11insG
XM_011539982.1:c.705+10_705+11insG XP_011538284.1:n.705+10_705+11insG
XR_945791.1:n.1371+10_1371+11insG
NM_000314.7:c.801+10_801+11insG NP_000305.3:n.801+10_801+11insG
NM_001304717.5:c.1320+10_1320+11insG NP_001291646.4:n.1320+10_1320+11insG
NM_001304718.2:c.210+10_210+11insG NP_001291647.1:n.210+10_210+11insG
NM_000314.8:c.801+10_801+11insG MANE Select NP_000305.3:n.801+10_801+11insG
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