Canonical Allele Identifier: CA379958833

Gene: WT1

Linked Data - Expert Curation

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392014C>G , CM000673.2:g.32392014C>G	GRCh38
NC_000011.9:g.32413560C>G , CM000673.1:g.32413560C>G	GRCh37
NC_000011.8:g.32370136C>G	NCBI36
NG_009272.1:g.48528G>C , LRG_525:g.48528G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1354G>C	ENSP00000331327.5:p.Asp452His
ENST00000379077.9:c.*589G>C	ENSP00000368368.5:n.*589G>C
ENST00000379079.8:c.754G>C	ENSP00000368370.2:p.Asp252His
ENST00000448076.9:c.1405G>C	ENSP00000413452.5:p.Asp469His
ENST00000452863.10:c.1405G>C MANE Select	ENSP00000415516.5:p.Asp469His
ENST00000526685.2:n.859G>C
ENST00000639563.3:c.1354G>C	ENSP00000492269.3:p.Asp452His
ENST00000639907.2:n.548G>C
ENST00000640146.2:c.730G>C	ENSP00000491984.2:p.Asp244His
ENST00000650745.1:n.1215G>C
ENST00000650861.1:n.1986G>C
ENST00000650986.1:n.68G>C
ENST00000651459.1:c.176G>C
ENST00000651533.1:n.451G>C
ENST00000651668.1:n.342G>C
ENST00000651794.1:n.1248G>C
ENST00000651819.1:n.330G>C
ENST00000652579.1:n.665G>C
ENST00000652724.1:n.595G>C
ENST00000332351.7:c.1390G>C	ENSP00000331327.3:p.Asp464His
ENST00000379077.7:c.*589G>C	ENSP00000368368.3:n.*589G>C
ENST00000379079.6:c.754G>C	ENSP00000368370.2:p.Asp252His
ENST00000448076.7:c.1390G>C	ENSP00000413452.3:p.Asp464His
ENST00000452863.7:c.1339G>C	ENSP00000415516.3:p.Asp447His
ENST00000527882.5:c.371G>C
ENST00000530998.5:c.703G>C	ENSP00000435307.1:p.Asp235His
NM_000378.4:c.1339G>C	NP_000369.3:p.Asp447His
NM_001198551.1:c.754G>C , LRG_525t2:c.754G>C	NP_001185480.1:p.Asp252His
NM_001198552.1:c.703G>C	NP_001185481.1:p.Asp235His
NM_024424.3:c.1390G>C	NP_077742.2:p.Asp464His
NM_024426.4:c.1390G>C	NP_077744.3:p.Asp464His
NM_000378.5:c.1354G>C	NP_000369.4:p.Asp452His
NM_024424.4:c.1405G>C	NP_077742.3:p.Asp469His
NM_024426.5:c.1405G>C	NP_077744.4:p.Asp469His
NM_001367854.1:c.217G>C	NP_001354783.1:p.Asp73His
NR_160306.1:n.1737G>C
NM_000378.6:c.1354G>C	NP_000369.4:p.Asp452His
NM_001198552.2:c.703G>C	NP_001185481.1:p.Asp235His
NM_024424.5:c.1405G>C	NP_077742.3:p.Asp469His
NM_024426.6:c.1405G>C MANE Select	NP_077744.4:p.Asp469His