LDH info

Canonical Allele Identifier: CA158221524
Gene: IKZF1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10235796

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.50394939T>C , CM000669.2:g.50394939T>C GRCh38
NC_000007.13:g.50462637T>C , CM000669.1:g.50462637T>C GRCh37
NC_000007.12:g.50430131T>C NCBI36
NG_034231.1:g.95857T>C

Transcript Alleles

HGVS Amino-acid change
NM_001220765.2:c.724+3076T>C VV NP_001207694.1:p.=
NM_001220767.2:c.559+3106T>C VV NP_001207696.1:p.=
NM_001220768.2:c.590-4979T>C VV NP_001207697.1:p.=
NM_001220770.2:c.433+3106T>C VV NP_001207699.1:p.=
NM_001220771.2:c.422-4979T>C VV NP_001207700.1:p.=
NM_001291837.1:c.724+3076T>C VV NP_001278766.1:p.=
NM_001291838.1:c.589+3076T>C VV NP_001278767.1:p.=
NM_001291839.1:c.463+3076T>C VV NP_001278768.1:p.=
NM_001291840.1:c.161-4979T>C VV NP_001278769.1:p.=
NM_001291841.1:c.421+3076T>C VV NP_001278770.1:p.=
NM_001291842.1:c.391+3106T>C VV NP_001278771.1:p.=
NM_001291843.1:c.295+3076T>C VV NP_001278772.1:p.=
NM_001291844.1:c.265+3106T>C VV NP_001278773.1:p.=
NM_006060.5:c.850+3076T>C VV NP_006051.1:p.=
XM_011515058.1:c.982+3076T>C XP_011513360.1:p.=
XM_011515059.1:c.952+3106T>C XP_011513361.1:p.=
XM_011515060.1:c.940+3076T>C XP_011513362.1:p.=
XM_011515061.1:c.922+3076T>C XP_011513363.1:p.=
XM_011515062.1:c.910+3076T>C XP_011513364.1:p.=
XM_011515063.1:c.910+3076T>C XP_011513365.1:p.=
XM_011515064.1:c.910+3076T>C XP_011513366.1:p.=
XM_011515065.1:c.910+3076T>C XP_011513367.1:p.=
XM_011515066.1:c.910+3076T>C XP_011513368.1:p.=
XM_011515067.1:c.856+3076T>C XP_011513369.1:p.=
XM_011515068.1:c.850+3076T>C XP_011513370.1:p.=
XM_011515069.1:c.850+3076T>C XP_011513371.1:p.=
XM_011515070.1:c.796+3076T>C XP_011513372.1:p.=
XM_011515071.1:c.721+3076T>C XP_011513373.1:p.=
XM_011515072.1:c.661+3076T>C XP_011513374.1:p.=
XM_011515073.1:c.649+3076T>C XP_011513375.1:p.=
XM_011515074.1:c.631+3106T>C XP_011513376.1:p.=
XM_011515075.1:c.589+3076T>C XP_011513377.1:p.=
XM_011515076.1:c.589+3076T>C XP_011513378.1:p.=
XM_011515077.1:c.535+3076T>C XP_011513379.1:p.=
XM_011515078.1:c.505+3106T>C XP_011513380.1:p.=
XR_927257.1:n.4452A>G
NM_006060.6:c.850+3076T>C VV MANE Preferred NP_006051.1:p.=
XM_011515058.2:c.982+3076T>C XP_011513360.1:p.=
XM_011515059.3:c.952+3106T>C XP_011513361.1:p.=
XM_011515060.2:c.940+3076T>C XP_011513362.1:p.=
XM_011515061.3:c.922+3076T>C XP_011513363.1:p.=
XM_011515062.2:c.910+3076T>C XP_011513364.1:p.=
XM_011515063.2:c.910+3076T>C XP_011513365.1:p.=
XM_011515064.3:c.910+3076T>C XP_011513366.1:p.=
XM_011515065.2:c.910+3076T>C XP_011513367.1:p.=
XM_011515066.2:c.910+3076T>C XP_011513368.1:p.=
XM_011515067.3:c.856+3076T>C XP_011513369.1:p.=
XM_011515068.2:c.850+3076T>C XP_011513370.1:p.=
XM_011515069.2:c.850+3076T>C XP_011513371.1:p.=
XM_011515070.2:c.796+3076T>C XP_011513372.1:p.=
XM_011515071.2:c.721+3076T>C XP_011513373.1:p.=
XM_011515072.2:c.661+3076T>C XP_011513374.1:p.=
XM_011515073.2:c.649+3076T>C XP_011513375.1:p.=
XM_011515074.2:c.631+3106T>C XP_011513376.1:p.=
XM_011515075.2:c.589+3076T>C XP_011513377.1:p.=
XM_011515076.2:c.589+3076T>C XP_011513378.1:p.=
XM_011515077.2:c.535+3076T>C XP_011513379.1:p.=
XM_011515078.2:c.505+3106T>C XP_011513380.1:p.=
XM_017011667.1:c.649+3076T>C XP_016867156.1:p.=
XM_017011668.1:c.589+3076T>C XP_016867157.1:p.=
ENST00000331340.7:c.850+3076T>C ENSP00000331614.3:p.=
ENST00000343574.9:c.589+3076T>C ENSP00000342750.5:p.=
ENST00000346667.8:c.41-4979T>C ENSP00000340080.5:p.=
ENST00000349824.8:c.422-4979T>C ENSP00000342485.4:p.=
ENST00000357364.8:c.590-4979T>C ENSP00000349928.4:p.=
ENST00000359197.9:c.724+3076T>C ENSP00000352123.5:p.=
ENST00000426121.1:n.110-4979T>C ENSP00000409588.1:p.=
ENST00000438033.5:c.589+3076T>C ENSP00000396554.1:p.=
ENST00000439701.1:c.724+3076T>C ENSP00000413025.1:p.=
ENST00000440768.6:c.175+3076T>C ENSP00000401507.3:p.=
ENST00000471793.1:n.1069+3076T>C
ENST00000612658.4:c.295-5176T>C ENSP00000483016.1:p.=
ENST00000615491.4:c.301+3076T>C ENSP00000478368.1:p.=