Canonical Allele Identifier: CA379964774

Gene: WT1

Linked Data

• MyVariant Identifiers: chr11:g.32456381T>C (hg19) ; chr11:g.32434835T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32434835T>C , CM000673.2:g.32434835T>C	GRCh38
NC_000011.9:g.32456381T>C , CM000673.1:g.32456381T>C	GRCh37
NC_000011.8:g.32412957T>C	NCBI36
NG_009272.1:g.5707A>G , LRG_525:g.5707A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.526A>G	ENSP00000331327.5:p.Thr176Ala
ENST00000379077.9:c.526A>G	ENSP00000368368.5:p.Thr176Ala
ENST00000448076.9:c.526A>G	ENSP00000413452.5:p.Thr176Ala
ENST00000452863.10:c.526A>G MANE Select	ENSP00000415516.5:p.Thr176Ala
ENST00000639563.3:c.526A>G	ENSP00000492269.3:p.Thr176Ala
ENST00000332351.7:c.511A>G	ENSP00000331327.3:p.Thr171Ala
ENST00000379077.7:c.511A>G	ENSP00000368368.3:p.Thr171Ala
ENST00000448076.7:c.511A>G	ENSP00000413452.3:p.Thr171Ala
ENST00000452863.7:c.511A>G	ENSP00000415516.3:p.Thr171Ala
NM_000378.4:c.511A>G	NP_000369.3:p.Thr171Ala
NM_024424.3:c.511A>G	NP_077742.2:p.Thr171Ala
NM_024426.4:c.511A>G	NP_077744.3:p.Thr171Ala
NM_000378.5:c.526A>G	NP_000369.4:p.Thr176Ala
NM_024424.4:c.526A>G	NP_077742.3:p.Thr176Ala
NM_024426.5:c.526A>G	NP_077744.4:p.Thr176Ala
NR_160306.1:n.705A>G
NM_000378.6:c.526A>G	NP_000369.4:p.Thr176Ala
NM_024424.5:c.526A>G	NP_077742.3:p.Thr176Ala
NM_024426.6:c.526A>G MANE Select	NP_077744.4:p.Thr176Ala