Canonical Allele Identifier: CA473565761

Gene: WT1

Linked Data

• gnomAD v4: 11-32392678-T-G
• MyVariant Identifiers: chr11:g.32414224T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392678T>G , CM000673.2:g.32392678T>G	GRCh38
NC_000011.9:g.32414224T>G , CM000673.1:g.32414224T>G	GRCh37
NC_000011.8:g.32370800T>G	NCBI36
NG_009272.1:g.47864A>C , LRG_525:g.47864A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1291A>C	ENSP00000331327.5:p.Arg431=
ENST00000379077.9:c.*526A>C	ENSP00000368368.5:n.*526A>C
ENST00000379079.8:c.691A>C	ENSP00000368370.2:p.Arg231=
ENST00000448076.9:c.1342A>C	ENSP00000413452.5:p.Arg448=
ENST00000452863.10:c.1342A>C MANE Select	ENSP00000415516.5:p.Arg448=
ENST00000526685.2:n.796A>C
ENST00000639563.3:c.1291A>C	ENSP00000492269.3:p.Arg431=
ENST00000639907.2:n.485A>C
ENST00000640146.2:c.667A>C	ENSP00000491984.2:p.Arg223=
ENST00000650745.1:n.551A>C
ENST00000650861.1:n.1923A>C
ENST00000651459.1:c.113A>C
ENST00000651533.1:n.388A>C
ENST00000651668.1:n.279A>C
ENST00000651794.1:n.1185A>C
ENST00000651819.1:n.267A>C
ENST00000652579.1:n.602A>C
ENST00000652724.1:n.532A>C
ENST00000332351.7:c.1327A>C	ENSP00000331327.3:p.Arg443=
ENST00000379077.7:c.*526A>C	ENSP00000368368.3:n.*526A>C
ENST00000379079.6:c.691A>C	ENSP00000368370.2:p.Arg231=
ENST00000448076.7:c.1327A>C	ENSP00000413452.3:p.Arg443=
ENST00000452863.7:c.1276A>C	ENSP00000415516.3:p.Arg426=
ENST00000527882.5:c.321-614A>C
ENST00000530998.5:c.640A>C	ENSP00000435307.1:p.Arg214=
NM_000378.4:c.1276A>C	NP_000369.3:p.Arg426=
NM_001198551.1:c.691A>C , LRG_525t2:c.691A>C	NP_001185480.1:p.Arg231=
NM_001198552.1:c.640A>C	NP_001185481.1:p.Arg214=
NM_024424.3:c.1327A>C	NP_077742.2:p.Arg443=
NM_024426.4:c.1327A>C	NP_077744.3:p.Arg443=
NM_000378.5:c.1291A>C	NP_000369.4:p.Arg431=
NM_024424.4:c.1342A>C	NP_077742.3:p.Arg448=
NM_024426.5:c.1342A>C	NP_077744.4:p.Arg448=
NM_001367854.1:c.154A>C	NP_001354783.1:p.Arg52=
NR_160306.1:n.1674A>C
NM_000378.6:c.1291A>C	NP_000369.4:p.Arg431=
NM_001198552.2:c.640A>C	NP_001185481.1:p.Arg214=
NM_024424.5:c.1342A>C	NP_077742.3:p.Arg448=
NM_024426.6:c.1342A>C MANE Select	NP_077744.4:p.Arg448=