Canonical Allele Identifier: CA016491

Gene: WT1

Linked Data

• ClinVar Variation Id: 198591
• ClinVar RCV Id: RCV003588590
• dbSNP Id: rs16754
• ExAC: 11:32417945 T / C
• gnomAD v2: 11-32417945-T-C
• gnomAD v3: 11-32396399-T-C
• gnomAD v4: 11-32396399-T-C
• MyVariant Identifiers: chr11:g.32417945T>C (hg19) ; chr11:g.32396399T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32396399T>C , CM000673.2:g.32396399T>C	GRCh38
NC_000011.9:g.32417945T>C , CM000673.1:g.32417945T>C	GRCh37
NC_000011.8:g.32374521T>C	NCBI36
NG_009272.1:g.44143A>G , LRG_525:g.44143A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1071A>G	ENSP00000331327.5:p.Arg357=
ENST00000379077.9:c.*306A>G	ENSP00000368368.5:n.*306A>G
ENST00000379079.8:c.471A>G	ENSP00000368370.2:p.Arg157=
ENST00000448076.9:c.1122A>G	ENSP00000413452.5:p.Arg374=
ENST00000452863.10:c.1122A>G MANE Select	ENSP00000415516.5:p.Arg374=
ENST00000526685.2:n.576A>G
ENST00000639563.3:c.1071A>G	ENSP00000492269.3:p.Arg357=
ENST00000639907.2:n.265A>G
ENST00000640146.2:c.447A>G	ENSP00000491984.2:p.Arg149=
ENST00000650861.1:n.1703A>G
ENST00000651459.1:c.35+3549A>G
ENST00000651668.1:n.59A>G
ENST00000651794.1:n.865A>G
ENST00000651819.1:n.47A>G
ENST00000652579.1:n.282A>G
ENST00000652724.1:n.312A>G
ENST00000332351.7:c.1107A>G	ENSP00000331327.3:p.Arg369=
ENST00000379077.7:c.*306A>G	ENSP00000368368.3:n.*306A>G
ENST00000379079.6:c.471A>G	ENSP00000368370.2:p.Arg157=
ENST00000448076.7:c.1107A>G	ENSP00000413452.3:p.Arg369=
ENST00000452863.7:c.1056A>G	ENSP00000415516.3:p.Arg352=
ENST00000526685.1:c.-67A>G	ENSP00000436292.1:n.-67A>G
ENST00000527775.1:c.360A>G	ENSP00000435351.1:p.Arg120=
ENST00000527882.5:c.178A>G
ENST00000530998.5:c.420A>G	ENSP00000435307.1:p.Arg140=
NM_000378.4:c.1056A>G	NP_000369.3:p.Arg352=
NM_001198551.1:c.471A>G , LRG_525t2:c.471A>G	NP_001185480.1:p.Arg157=
NM_001198552.1:c.420A>G	NP_001185481.1:p.Arg140=
NM_024424.3:c.1107A>G	NP_077742.2:p.Arg369=
NM_024426.4:c.1107A>G	NP_077744.3:p.Arg369=
NM_000378.5:c.1071A>G	NP_000369.4:p.Arg357=
NM_024424.4:c.1122A>G	NP_077742.3:p.Arg374=
NM_024426.5:c.1122A>G	NP_077744.4:p.Arg374=
NM_001367854.1:c.-67A>G	NP_001354783.1:n.-67A>G
NR_160306.1:n.1454A>G
NM_000378.6:c.1071A>G	NP_000369.4:p.Arg357=
NM_001198552.2:c.420A>G	NP_001185481.1:p.Arg140=
NM_024424.5:c.1122A>G	NP_077742.3:p.Arg374=
NM_024426.6:c.1122A>G MANE Select	NP_077744.4:p.Arg374=