Canonical Allele Identifier: CA595184741
Gene: PTEN HGNC NCBI

Linked Data

dbSNP Id: rs1186087266
gnomAD v2: 10-89717828-A-ATC
MyVariant Identifiers: chr10:g.89717828_89717829insTC (hg19) chr10:g.87958071_87958072insTC (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87958071_87958072insTC , CM000672.2:g.87958071_87958072insTC GRCh38
NC_000010.10:g.89717828_89717829insTC , CM000672.1:g.89717828_89717829insTC GRCh37
NC_000010.9:g.89707808_89707809insTC NCBI36
NG_007466.2:g.99633_99634insTC , LRG_311:g.99633_99634insTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.801+52_801+53insTC ENSP00000514759.2:n.801+52_801+53insTC
ENST00000710265.1:c.801+52_801+53insTC ENSP00000518161.1:n.801+52_801+53insTC
ENST00000472832.3:c.801+52_801+53insTC ENSP00000483066.2:n.801+52_801+53insTC
ENST00000688158.2:n.1536+52_1536+53insTC
ENST00000688922.2:c.*631+52_*631+53insTC ENSP00000508742.2:n.*631+52_*631+53insTC
ENST00000700021.1:c.756+52_756+53insTC ENSP00000514757.1:n.756+52_756+53insTC
ENST00000700022.1:c.*140+52_*140+53insTC ENSP00000514758.1:n.*140+52_*140+53insTC
ENST00000700023.1:n.1959+52_1959+53insTC
ENST00000700024.1:n.2193+52_2193+53insTC
ENST00000700025.1:n.1570+52_1570+53insTC
ENST00000700026.1:n.438+52_438+53insTC
ENST00000700029.1:c.635+52_635+53insTC
ENST00000706954.1:c.801+52_801+53insTC ENSP00000516674.1:n.801+52_801+53insTC
ENST00000706955.1:c.*836+52_*836+53insTC ENSP00000516675.1:n.*836+52_*836+53insTC
ENST00000686459.1:c.*387+52_*387+53insTC ENSP00000508909.1:n.*387+52_*387+53insTC
ENST00000688158.1:c.*912+52_*912+53insTC ENSP00000509254.1:n.*912+52_*912+53insTC
ENST00000688308.1:c.801+52_801+53insTC ENSP00000508752.1:n.801+52_801+53insTC
ENST00000688922.1:c.722+52_722+53insTC
ENST00000693560.1:c.1320+52_1320+53insTC ENSP00000509861.1:n.1320+52_1320+53insTC
ENST00000371953.8:c.801+52_801+53insTC MANE Select ENSP00000361021.3:n.801+52_801+53insTC
ENST00000371953.7:c.801+52_801+53insTC ENSP00000361021.3:n.801+52_801+53insTC
ENST00000472832.2:c.228+52_228+53insTC ENSP00000483066.1:n.228+52_228+53insTC
NM_000314.5:c.801+52_801+53insTC NP_000305.3:n.801+52_801+53insTC
NM_000314.6:c.801+52_801+53insTC NP_000305.3:n.801+52_801+53insTC
NM_001304717.2:c.1320+52_1320+53insTC NP_001291646.2:n.1320+52_1320+53insTC
NM_001304718.1:c.210+52_210+53insTC NP_001291647.1:n.210+52_210+53insTC
XM_006717926.2:c.756+52_756+53insTC XP_006717989.1:n.756+52_756+53insTC
XM_011539981.1:c.801+52_801+53insTC XP_011538283.1:n.801+52_801+53insTC
XM_011539982.1:c.705+52_705+53insTC XP_011538284.1:n.705+52_705+53insTC
XR_945791.1:n.1371+52_1371+53insTC
NM_000314.7:c.801+52_801+53insTC NP_000305.3:n.801+52_801+53insTC
NM_001304717.5:c.1320+52_1320+53insTC NP_001291646.4:n.1320+52_1320+53insTC
NM_001304718.2:c.210+52_210+53insTC NP_001291647.1:n.210+52_210+53insTC
NM_000314.8:c.801+52_801+53insTC MANE Select NP_000305.3:n.801+52_801+53insTC
Search 100 bp 5'
Search 100 bp 3'