Canonical Allele Identifier: CA379966252

Gene: WT1

Linked Data

• ClinVar Variation Id: 1809679
• ClinVar RCV Id: RCV002496211
• gnomAD v4: 11-32435198-C-T
• MyVariant Identifiers: chr11:g.32456744C>T (hg19) ; chr11:g.32435198C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32435198C>T , CM000673.2:g.32435198C>T	GRCh38
NC_000011.9:g.32456744C>T , CM000673.1:g.32456744C>T	GRCh37
NC_000011.8:g.32413320C>T	NCBI36
NG_009272.1:g.5344G>A , LRG_525:g.5344G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.163G>A	ENSP00000331327.5:p.Ala55Thr
ENST00000379077.9:c.163G>A	ENSP00000368368.5:p.Ala55Thr
ENST00000448076.9:c.163G>A	ENSP00000413452.5:p.Ala55Thr
ENST00000452863.10:c.163G>A MANE Select	ENSP00000415516.5:p.Ala55Thr
ENST00000639563.3:c.163G>A	ENSP00000492269.3:p.Ala55Thr
ENST00000332351.7:c.148G>A	ENSP00000331327.3:p.Ala50Thr
ENST00000379077.7:c.148G>A	ENSP00000368368.3:p.Ala50Thr
ENST00000448076.7:c.148G>A	ENSP00000413452.3:p.Ala50Thr
ENST00000452863.7:c.148G>A	ENSP00000415516.3:p.Ala50Thr
NM_000378.4:c.148G>A	NP_000369.3:p.Ala50Thr
NM_024424.3:c.148G>A	NP_077742.2:p.Ala50Thr
NM_024426.4:c.148G>A	NP_077744.3:p.Ala50Thr
NM_000378.5:c.163G>A	NP_000369.4:p.Ala55Thr
NM_024424.4:c.163G>A	NP_077742.3:p.Ala55Thr
NM_024426.5:c.163G>A	NP_077744.4:p.Ala55Thr
NR_160306.1:n.342G>A
NM_000378.6:c.163G>A	NP_000369.4:p.Ala55Thr
NM_024424.5:c.163G>A	NP_077742.3:p.Ala55Thr
NM_024426.6:c.163G>A MANE Select	NP_077744.4:p.Ala55Thr