Canonical Allele Identifier: CA379958886

Gene: WT1

Linked Data

• COSMIC: COSM270558
• MyVariant Identifiers: chr11:g.32413574T>G (hg19) ; chr11:g.32392028T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392028T>G , CM000673.2:g.32392028T>G	GRCh38
NC_000011.9:g.32413574T>G , CM000673.1:g.32413574T>G	GRCh37
NC_000011.8:g.32370150T>G	NCBI36
NG_009272.1:g.48514A>C , LRG_525:g.48514A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1340A>C	ENSP00000331327.5:p.Lys447Thr
ENST00000379077.9:c.*575A>C	ENSP00000368368.5:n.*575A>C
ENST00000379079.8:c.740A>C	ENSP00000368370.2:p.Lys247Thr
ENST00000448076.9:c.1391A>C	ENSP00000413452.5:p.Lys464Thr
ENST00000452863.10:c.1391A>C MANE Select	ENSP00000415516.5:p.Lys464Thr
ENST00000526685.2:n.845A>C
ENST00000639563.3:c.1340A>C	ENSP00000492269.3:p.Lys447Thr
ENST00000639907.2:n.534A>C
ENST00000640146.2:c.716A>C	ENSP00000491984.2:p.Lys239Thr
ENST00000650745.1:n.1201A>C
ENST00000650861.1:n.1972A>C
ENST00000650986.1:n.54A>C
ENST00000651459.1:c.162A>C
ENST00000651533.1:n.437A>C
ENST00000651668.1:n.328A>C
ENST00000651794.1:n.1234A>C
ENST00000651819.1:n.316A>C
ENST00000652579.1:n.651A>C
ENST00000652724.1:n.581A>C
ENST00000332351.7:c.1376A>C	ENSP00000331327.3:p.Lys459Thr
ENST00000379077.7:c.*575A>C	ENSP00000368368.3:n.*575A>C
ENST00000379079.6:c.740A>C	ENSP00000368370.2:p.Lys247Thr
ENST00000448076.7:c.1376A>C	ENSP00000413452.3:p.Lys459Thr
ENST00000452863.7:c.1325A>C	ENSP00000415516.3:p.Lys442Thr
ENST00000527882.5:c.357A>C
ENST00000530998.5:c.689A>C	ENSP00000435307.1:p.Lys230Thr
NM_000378.4:c.1325A>C	NP_000369.3:p.Lys442Thr
NM_001198551.1:c.740A>C , LRG_525t2:c.740A>C	NP_001185480.1:p.Lys247Thr
NM_001198552.1:c.689A>C	NP_001185481.1:p.Lys230Thr
NM_024424.3:c.1376A>C	NP_077742.2:p.Lys459Thr
NM_024426.4:c.1376A>C	NP_077744.3:p.Lys459Thr
NM_000378.5:c.1340A>C	NP_000369.4:p.Lys447Thr
NM_024424.4:c.1391A>C	NP_077742.3:p.Lys464Thr
NM_024426.5:c.1391A>C	NP_077744.4:p.Lys464Thr
NM_001367854.1:c.203A>C	NP_001354783.1:p.Lys68Thr
NR_160306.1:n.1723A>C
NM_000378.6:c.1340A>C	NP_000369.4:p.Lys447Thr
NM_001198552.2:c.689A>C	NP_001185481.1:p.Lys230Thr
NM_024424.5:c.1391A>C	NP_077742.3:p.Lys464Thr
NM_024426.6:c.1391A>C MANE Select	NP_077744.4:p.Lys464Thr