Canonical Allele Identifier: CA470669906
Gene: PTEN HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.89717731_89717732insC (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957974_87957975insC , CM000672.2:g.87957974_87957975insC GRCh38
NC_000010.10:g.89717731_89717732insC , CM000672.1:g.89717731_89717732insC GRCh37
NC_000010.9:g.89707711_89707712insC NCBI36
NG_007466.2:g.99536_99537insC , LRG_311:g.99536_99537insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.756_757insC ENSP00000514759.2:p.Ile253HisfsTer?
ENST00000710265.1:c.756_757insC ENSP00000518161.1:p.Ile253HisfsTer?
ENST00000472832.3:c.756_757insC ENSP00000483066.2:p.Ile253HisfsTer?
ENST00000688158.2:n.1491_1492insC
ENST00000688922.2:c.*586_*587insC ENSP00000508742.2:n.*586_*587insC
ENST00000700021.1:c.711_712insC ENSP00000514757.1:p.Ile238HisfsTer?
ENST00000700022.1:c.*95_*96insC ENSP00000514758.1:n.*95_*96insC
ENST00000700023.1:n.1914_1915insC
ENST00000700024.1:n.2148_2149insC
ENST00000700025.1:n.1525_1526insC
ENST00000700026.1:n.393_394insC
ENST00000700029.1:c.590_591insC
ENST00000706954.1:c.756_757insC ENSP00000516674.1:p.Ile253HisfsTer?
ENST00000706955.1:c.*791_*792insC ENSP00000516675.1:n.*791_*792insC
ENST00000686459.1:c.*342_*343insC ENSP00000508909.1:n.*342_*343insC
ENST00000688158.1:c.*867_*868insC ENSP00000509254.1:n.*867_*868insC
ENST00000688308.1:c.756_757insC ENSP00000508752.1:p.Ile253HisfsTer?
ENST00000688922.1:c.677_678insC
ENST00000693560.1:c.1275_1276insC ENSP00000509861.1:p.Ile426HisfsTer?
ENST00000371953.8:c.756_757insC MANE Select ENSP00000361021.3:p.Ile253HisfsTer?
ENST00000371953.7:c.756_757insC ENSP00000361021.3:p.Ile253HisfsTer?
ENST00000472832.2:c.183_184insC ENSP00000483066.1:p.Ile62HisfsTer?
NM_000314.5:c.756_757insC NP_000305.3:p.Ile253HisfsTer?
NM_000314.6:c.756_757insC NP_000305.3:p.Ile253HisfsTer?
NM_001304717.2:c.1275_1276insC NP_001291646.2:p.Ile426HisfsTer?
NM_001304718.1:c.165_166insC NP_001291647.1:p.Ile56HisfsTer?
XM_006717926.2:c.711_712insC XP_006717989.1:p.Ile238HisfsTer?
XM_011539981.1:c.756_757insC XP_011538283.1:p.Ile253HisfsTer?
XM_011539982.1:c.660_661insC XP_011538284.1:p.Ile221HisfsTer?
XR_945791.1:n.1326_1327insC
NM_000314.7:c.756_757insC NP_000305.3:p.Ile253HisfsTer?
NM_001304717.5:c.1275_1276insC NP_001291646.4:p.Ile426HisfsTer?
NM_001304718.2:c.165_166insC NP_001291647.1:p.Ile56HisfsTer?
NM_000314.8:c.756_757insC MANE Select NP_000305.3:p.Ile253HisfsTer?
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