Canonical Allele Identifier: CA379960389

Gene: WT1

Linked Data

• MyVariant Identifiers: chr11:g.32421540C>G (hg19) ; chr11:g.32399994C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32399994C>G , CM000673.2:g.32399994C>G	GRCh38
NC_000011.9:g.32421540C>G , CM000673.1:g.32421540C>G	GRCh37
NC_000011.8:g.32378116C>G	NCBI36
NG_009272.1:g.40548G>C , LRG_525:g.40548G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1016G>C	ENSP00000331327.5:p.Gly339Ala
ENST00000379077.9:c.*251G>C	ENSP00000368368.5:n.*251G>C
ENST00000379079.8:c.416G>C	ENSP00000368370.2:p.Gly139Ala
ENST00000448076.9:c.1067G>C	ENSP00000413452.5:p.Gly356Ala
ENST00000452863.10:c.1067G>C MANE Select	ENSP00000415516.5:p.Gly356Ala
ENST00000526685.2:n.521G>C
ENST00000639563.3:c.1016G>C	ENSP00000492269.3:p.Gly339Ala
ENST00000639907.2:n.210G>C
ENST00000640146.2:c.392G>C	ENSP00000491984.2:p.Gly131Ala
ENST00000651794.1:n.810G>C
ENST00000652579.1:n.227G>C
ENST00000652724.1:n.257G>C
ENST00000332351.7:c.1052G>C	ENSP00000331327.3:p.Gly351Ala
ENST00000379077.7:c.*251G>C	ENSP00000368368.3:n.*251G>C
ENST00000379079.6:c.416G>C	ENSP00000368370.2:p.Gly139Ala
ENST00000448076.7:c.1052G>C	ENSP00000413452.3:p.Gly351Ala
ENST00000452863.7:c.1001G>C	ENSP00000415516.3:p.Gly334Ala
ENST00000526685.1:c.-122G>C	ENSP00000436292.1:n.-122G>C
ENST00000527775.1:c.305G>C	ENSP00000435351.1:p.Gly102Ala
ENST00000527882.5:c.123G>C
ENST00000530998.5:c.365G>C	ENSP00000435307.1:p.Gly122Ala
NM_000378.4:c.1001G>C	NP_000369.3:p.Gly334Ala
NM_001198551.1:c.416G>C , LRG_525t2:c.416G>C	NP_001185480.1:p.Gly139Ala
NM_001198552.1:c.365G>C	NP_001185481.1:p.Gly122Ala
NM_024424.3:c.1052G>C	NP_077742.2:p.Gly351Ala
NM_024426.4:c.1052G>C	NP_077744.3:p.Gly351Ala
NM_000378.5:c.1016G>C	NP_000369.4:p.Gly339Ala
NM_024424.4:c.1067G>C	NP_077742.3:p.Gly356Ala
NM_024426.5:c.1067G>C	NP_077744.4:p.Gly356Ala
NM_001367854.1:c.-122G>C	NP_001354783.1:n.-122G>C
NR_160306.1:n.1399G>C
NM_000378.6:c.1016G>C	NP_000369.4:p.Gly339Ala
NM_001198552.2:c.365G>C	NP_001185481.1:p.Gly122Ala
NM_024424.5:c.1067G>C	NP_077742.3:p.Gly356Ala
NM_024426.6:c.1067G>C MANE Select	NP_077744.4:p.Gly356Ala