Canonical Allele Identifier: CA1126018548
Gene: TLE1 HGNC NCBI

Linked Data

dbSNP Id: rs199731120

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.81680949_81680950dup , CM000671.2:g.81680949_81680950dup GRCh38
NC_000009.11:g.84295864_84295865dup , CM000671.1:g.84295864_84295865dup GRCh37
NC_000009.10:g.83485684_83485685dup NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000376463.3:c.144+4732_144+4733dup ENSP00000365646.2:n.144+4732_144+4733dup
ENST00000376499.8:c.234+4732_234+4733dup MANE Select ENSP00000365682.3:n.234+4732_234+4733dup
ENST00000674113.1:c.109+4732_109+4733dup
ENST00000376463.2:c.66+4732_66+4733dup ENSP00000365646.1:n.66+4732_66+4733dup
ENST00000376472.5:c.234+4732_234+4733dup ENSP00000365655.2:n.234+4732_234+4733dup
ENST00000376499.7:c.234+4732_234+4733dup ENSP00000365682.3:n.234+4732_234+4733dup
ENST00000418319.5:c.234+4732_234+4733dup ENSP00000391347.1:n.234+4732_234+4733dup
NM_001303103.1:c.234+4732_234+4733dup NP_001290032.1:n.234+4732_234+4733dup
NM_001303104.1:c.234+4732_234+4733dup NP_001290033.1:n.234+4732_234+4733dup
NM_005077.4:c.234+4732_234+4733dup NP_005068.2:n.234+4732_234+4733dup
XM_005252151.1:c.234+4732_234+4733dup XP_005252208.1:n.234+4732_234+4733dup
XM_005252152.1:c.234+4732_234+4733dup XP_005252209.1:n.234+4732_234+4733dup
XM_005252153.1:c.234+4732_234+4733dup XP_005252210.1:n.234+4732_234+4733dup
XM_005252154.1:c.234+4732_234+4733dup XP_005252211.1:n.234+4732_234+4733dup
XM_005252156.1:c.234+4732_234+4733dup XP_005252213.1:n.234+4732_234+4733dup
XM_005252162.1:c.234+4732_234+4733dup XP_005252219.1:n.234+4732_234+4733dup
XM_005252163.1:c.234+4732_234+4733dup XP_005252220.1:n.234+4732_234+4733dup
XM_006717258.1:c.234+4732_234+4733dup XP_006717321.1:n.234+4732_234+4733dup
XM_006717259.2:c.234+4732_234+4733dup XP_006717322.1:n.234+4732_234+4733dup
XM_006717260.1:c.234+4732_234+4733dup XP_006717323.1:n.234+4732_234+4733dup
XM_006717261.2:c.-222+4732_-222+4733dup XP_006717324.1:n.-222+4732_-222+4733dup
XM_006717262.1:c.234+4732_234+4733dup XP_006717325.1:n.234+4732_234+4733dup
XM_006717263.1:c.234+4732_234+4733dup XP_006717326.1:n.234+4732_234+4733dup
XM_011518951.1:c.234+4732_234+4733dup XP_011517253.1:n.234+4732_234+4733dup
XM_005252156.3:c.234+4732_234+4733dup XP_005252213.1:n.234+4732_234+4733dup
XM_005252163.2:c.234+4732_234+4733dup XP_005252220.1:n.234+4732_234+4733dup
XM_006717259.4:c.234+4732_234+4733dup XP_006717322.1:n.234+4732_234+4733dup
XM_011518951.2:c.234+4732_234+4733dup XP_011517253.1:n.234+4732_234+4733dup
XM_017015064.1:c.234+4732_234+4733dup XP_016870553.1:n.234+4732_234+4733dup
XM_017015065.1:c.234+4732_234+4733dup XP_016870554.1:n.234+4732_234+4733dup
XM_017015066.1:c.234+4732_234+4733dup XP_016870555.1:n.234+4732_234+4733dup
NM_005077.5:c.234+4732_234+4733dup MANE Select NP_005068.2:n.234+4732_234+4733dup
NM_001303103.2:c.234+4732_234+4733dup NP_001290032.1:n.234+4732_234+4733dup
NM_001303104.2:c.234+4732_234+4733dup NP_001290033.1:n.234+4732_234+4733dup