Canonical Allele Identifier: CA379960324

Gene: WT1

Linked Data

• MyVariant Identifiers: chr11:g.32421522T>C (hg19) ; chr11:g.32399976T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32399976T>C , CM000673.2:g.32399976T>C	GRCh38
NC_000011.9:g.32421522T>C , CM000673.1:g.32421522T>C	GRCh37
NC_000011.8:g.32378098T>C	NCBI36
NG_009272.1:g.40566A>G , LRG_525:g.40566A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1034A>G	ENSP00000331327.5:p.His345Arg
ENST00000379077.9:c.*269A>G	ENSP00000368368.5:n.*269A>G
ENST00000379079.8:c.434A>G	ENSP00000368370.2:p.His145Arg
ENST00000448076.9:c.1085A>G	ENSP00000413452.5:p.His362Arg
ENST00000452863.10:c.1085A>G MANE Select	ENSP00000415516.5:p.His362Arg
ENST00000526685.2:n.539A>G
ENST00000639563.3:c.1034A>G	ENSP00000492269.3:p.His345Arg
ENST00000639907.2:n.228A>G
ENST00000640146.2:c.410A>G	ENSP00000491984.2:p.His137Arg
ENST00000651459.1:c.7A>G
ENST00000651794.1:n.828A>G
ENST00000652579.1:n.245A>G
ENST00000652724.1:n.275A>G
ENST00000332351.7:c.1070A>G	ENSP00000331327.3:p.His357Arg
ENST00000379077.7:c.*269A>G	ENSP00000368368.3:n.*269A>G
ENST00000379079.6:c.434A>G	ENSP00000368370.2:p.His145Arg
ENST00000448076.7:c.1070A>G	ENSP00000413452.3:p.His357Arg
ENST00000452863.7:c.1019A>G	ENSP00000415516.3:p.His340Arg
ENST00000526685.1:c.-104A>G	ENSP00000436292.1:n.-104A>G
ENST00000527775.1:c.323A>G	ENSP00000435351.1:p.His108Arg
ENST00000527882.5:c.141A>G
ENST00000530998.5:c.383A>G	ENSP00000435307.1:p.His128Arg
NM_000378.4:c.1019A>G	NP_000369.3:p.His340Arg
NM_001198551.1:c.434A>G , LRG_525t2:c.434A>G	NP_001185480.1:p.His145Arg
NM_001198552.1:c.383A>G	NP_001185481.1:p.His128Arg
NM_024424.3:c.1070A>G	NP_077742.2:p.His357Arg
NM_024426.4:c.1070A>G	NP_077744.3:p.His357Arg
NM_000378.5:c.1034A>G	NP_000369.4:p.His345Arg
NM_024424.4:c.1085A>G	NP_077742.3:p.His362Arg
NM_024426.5:c.1085A>G	NP_077744.4:p.His362Arg
NM_001367854.1:c.-104A>G	NP_001354783.1:n.-104A>G
NR_160306.1:n.1417A>G
NM_000378.6:c.1034A>G	NP_000369.4:p.His345Arg
NM_001198552.2:c.383A>G	NP_001185481.1:p.His128Arg
NM_024424.5:c.1085A>G	NP_077742.3:p.His362Arg
NM_024426.6:c.1085A>G MANE Select	NP_077744.4:p.His362Arg