Canonical Allele Identifier: CA473568316

Gene: WT1

Linked Data

• ClinVar Variation Id: 2942338
• ClinVar RCV Id: RCV003805552
• dbSNP Id: rs1268419525
• MyVariant Identifiers: chr11:g.32439158G>C (hg19) ; chr11:g.32417612G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32417612G>C , CM000673.2:g.32417612G>C	GRCh38
NC_000011.9:g.32439158G>C , CM000673.1:g.32439158G>C	GRCh37
NC_000011.8:g.32395734G>C	NCBI36
NG_009272.1:g.22930C>G , LRG_525:g.22930C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.930C>G	ENSP00000331327.5:p.Thr310=
ENST00000379077.9:c.930C>G	ENSP00000368368.5:p.Thr310=
ENST00000379079.8:c.279C>G	ENSP00000368370.2:p.Thr93=
ENST00000448076.9:c.930C>G	ENSP00000413452.5:p.Thr310=
ENST00000452863.10:c.930C>G MANE Select	ENSP00000415516.5:p.Thr310=
ENST00000639563.3:c.930C>G	ENSP00000492269.3:p.Thr310=
ENST00000640146.2:c.306C>G	ENSP00000491984.2:p.Thr102=
ENST00000332351.7:c.915C>G	ENSP00000331327.3:p.Thr305=
ENST00000379077.7:c.915C>G	ENSP00000368368.3:p.Thr305=
ENST00000379079.6:c.279C>G	ENSP00000368370.2:p.Thr93=
ENST00000448076.7:c.915C>G	ENSP00000413452.3:p.Thr305=
ENST00000452863.7:c.915C>G	ENSP00000415516.3:p.Thr305=
ENST00000527775.1:c.168C>G	ENSP00000435351.1:p.Thr56=
ENST00000530998.5:c.279C>G	ENSP00000435307.1:p.Thr93=
NM_000378.4:c.915C>G	NP_000369.3:p.Thr305=
NM_001198551.1:c.279C>G , LRG_525t2:c.279C>G	NP_001185480.1:p.Thr93=
NM_001198552.1:c.279C>G	NP_001185481.1:p.Thr93=
NM_024424.3:c.915C>G	NP_077742.2:p.Thr305=
NM_024426.4:c.915C>G	NP_077744.3:p.Thr305=
NM_000378.5:c.930C>G	NP_000369.4:p.Thr310=
NM_024424.4:c.930C>G	NP_077742.3:p.Thr310=
NM_024426.5:c.930C>G	NP_077744.4:p.Thr310=
NR_160306.1:n.1109C>G
NM_000378.6:c.930C>G	NP_000369.4:p.Thr310=
NM_001198552.2:c.279C>G	NP_001185481.1:p.Thr93=
NM_024424.5:c.930C>G	NP_077742.3:p.Thr310=
NM_024426.6:c.930C>G MANE Select	NP_077744.4:p.Thr310=