LDH info

Canonical Allele Identifier: CA016298
Gene: WT1 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 3495
dbSNP Id: rs28942089

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32392672G>A , CM000673.2:g.32392672G>A GRCh38
NC_000011.9:g.32414218G>A , CM000673.1:g.32414218G>A GRCh37
NC_000011.8:g.32370794G>A NCBI36
NG_009272.1:g.47870C>T , LRG_525:g.47870C>T

Transcript Alleles

HGVS Amino-acid change
NM_000378.4:c.1282C>T VV NP_000369.3:p.His428Tyr
NM_001198551.1:c.697C>T , LRG_525t2:c.697C>T NP_001185480.1:p.His233Tyr
NM_001198552.1:c.646C>T VV NP_001185481.1:p.His216Tyr
NM_024424.3:c.1333C>T VV NP_077742.2:p.His445Tyr
NM_024426.4:c.1333C>T VV NP_077744.3:p.His445Tyr
NM_000378.5:c.1297C>T VV NP_000369.4:p.His433Tyr
NM_024424.4:c.1348C>T VV NP_077742.3:p.His450Tyr
NM_024426.5:c.1348C>T VV NP_077744.4:p.His450Tyr
NM_001367854.1:c.160C>T VV NP_001354783.1:p.His54Tyr
NR_160306.1:n.1680C>T
ENST00000332351.7:c.1333C>T ENSP00000331327.3:p.His445Tyr
ENST00000379077.7:c.*532C>T ENSP00000368368.3:p.=
ENST00000379079.6:c.697C>T ENSP00000368370.2:p.His233Tyr
ENST00000448076.7:c.1333C>T ENSP00000413452.3:p.His445Tyr
ENST00000452863.7:n.1282C>T ENSP00000415516.3:p.His428Tyr
ENST00000527882.5:n.321-608C>T
ENST00000530998.5:c.646C>T ENSP00000435307.1:p.His216Tyr