Canonical Allele Identifier: CA379958870

Gene: WT1

Linked Data

• MyVariant Identifiers: chr11:g.32413571A>G (hg19) ; chr11:g.32392025A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392025A>G , CM000673.2:g.32392025A>G	GRCh38
NC_000011.9:g.32413571A>G , CM000673.1:g.32413571A>G	GRCh37
NC_000011.8:g.32370147A>G	NCBI36
NG_009272.1:g.48517T>C , LRG_525:g.48517T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1343T>C	ENSP00000331327.5:p.Phe448Ser
ENST00000379077.9:c.*578T>C	ENSP00000368368.5:n.*578T>C
ENST00000379079.8:c.743T>C	ENSP00000368370.2:p.Phe248Ser
ENST00000448076.9:c.1394T>C	ENSP00000413452.5:p.Phe465Ser
ENST00000452863.10:c.1394T>C MANE Select	ENSP00000415516.5:p.Phe465Ser
ENST00000526685.2:n.848T>C
ENST00000639563.3:c.1343T>C	ENSP00000492269.3:p.Phe448Ser
ENST00000639907.2:n.537T>C
ENST00000640146.2:c.719T>C	ENSP00000491984.2:p.Phe240Ser
ENST00000650745.1:n.1204T>C
ENST00000650861.1:n.1975T>C
ENST00000650986.1:n.57T>C
ENST00000651459.1:c.165T>C
ENST00000651533.1:n.440T>C
ENST00000651668.1:n.331T>C
ENST00000651794.1:n.1237T>C
ENST00000651819.1:n.319T>C
ENST00000652579.1:n.654T>C
ENST00000652724.1:n.584T>C
ENST00000332351.7:c.1379T>C	ENSP00000331327.3:p.Phe460Ser
ENST00000379077.7:c.*578T>C	ENSP00000368368.3:n.*578T>C
ENST00000379079.6:c.743T>C	ENSP00000368370.2:p.Phe248Ser
ENST00000448076.7:c.1379T>C	ENSP00000413452.3:p.Phe460Ser
ENST00000452863.7:c.1328T>C	ENSP00000415516.3:p.Phe443Ser
ENST00000527882.5:c.360T>C
ENST00000530998.5:c.692T>C	ENSP00000435307.1:p.Phe231Ser
NM_000378.4:c.1328T>C	NP_000369.3:p.Phe443Ser
NM_001198551.1:c.743T>C , LRG_525t2:c.743T>C	NP_001185480.1:p.Phe248Ser
NM_001198552.1:c.692T>C	NP_001185481.1:p.Phe231Ser
NM_024424.3:c.1379T>C	NP_077742.2:p.Phe460Ser
NM_024426.4:c.1379T>C	NP_077744.3:p.Phe460Ser
NM_000378.5:c.1343T>C	NP_000369.4:p.Phe448Ser
NM_024424.4:c.1394T>C	NP_077742.3:p.Phe465Ser
NM_024426.5:c.1394T>C	NP_077744.4:p.Phe465Ser
NM_001367854.1:c.206T>C	NP_001354783.1:p.Phe69Ser
NR_160306.1:n.1726T>C
NM_000378.6:c.1343T>C	NP_000369.4:p.Phe448Ser
NM_001198552.2:c.692T>C	NP_001185481.1:p.Phe231Ser
NM_024424.5:c.1394T>C	NP_077742.3:p.Phe465Ser
NM_024426.6:c.1394T>C MANE Select	NP_077744.4:p.Phe465Ser