LDH info

Canonical Allele Identifier: CA351790
Gene: WT1 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 222890
ClinVar RCV Id: RCV000208133
dbSNP Id: rs869025561

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32392755C>A , CM000673.2:g.32392755C>A GRCh38
NC_000011.9:g.32414301C>A , CM000673.1:g.32414301C>A GRCh37
NC_000011.8:g.32370877C>A NCBI36
NG_009272.1:g.47787G>T , LRG_525:g.47787G>T

Transcript Alleles

HGVS Amino-acid change
NM_000378.4:c.1199G>T VV NP_000369.3:p.Gly400Val
NM_001198551.1:c.614G>T , LRG_525t2:c.614G>T NP_001185480.1:p.Gly205Val
NM_001198552.1:c.563G>T VV NP_001185481.1:p.Gly188Val
NM_024424.3:c.1250G>T VV NP_077742.2:p.Gly417Val
NM_024426.4:c.1250G>T VV NP_077744.3:p.Gly417Val
NM_000378.5:c.1214G>T VV NP_000369.4:p.Gly405Val
NM_024424.4:c.1265G>T VV NP_077742.3:p.Gly422Val
NM_024426.5:c.1265G>T VV NP_077744.4:p.Gly422Val
NM_001367854.1:c.77G>T VV NP_001354783.1:p.Gly26Val
NR_160306.1:n.1597G>T
ENST00000332351.7:c.1250G>T ENSP00000331327.3:p.Gly417Val
ENST00000379077.7:c.*449G>T ENSP00000368368.3:p.=
ENST00000379079.6:c.614G>T ENSP00000368370.2:p.Gly205Val
ENST00000448076.7:c.1250G>T ENSP00000413452.3:p.Gly417Val
ENST00000452863.7:n.1199G>T ENSP00000415516.3:p.Gly400Val
ENST00000527882.5:n.321-691G>T
ENST00000530998.5:c.563G>T ENSP00000435307.1:p.Gly188Val