Canonical Allele Identifier: CA10634685

Gene: WT1

Linked Data

• ClinVar Variation Id: 304418
• ClinVar RCV Id: RCV000272000 ; RCV000310774 ; RCV000359651 ; RCV000897033 ; RCV003588613
• dbSNP Id: rs886048227
• gnomAD v4: 11-32396321-G-A
• MyVariant Identifiers: chr11:g.32417867G>A (hg19) ; chr11:g.32396321G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32396321G>A , CM000673.2:g.32396321G>A	GRCh38
NC_000011.9:g.32417867G>A , CM000673.1:g.32417867G>A	GRCh37
NC_000011.8:g.32374443G>A	NCBI36
NG_009272.1:g.44221C>T , LRG_525:g.44221C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1149C>T	ENSP00000331327.5:p.Tyr383=
ENST00000379077.9:c.*384C>T	ENSP00000368368.5:n.*384C>T
ENST00000379079.8:c.549C>T	ENSP00000368370.2:p.Tyr183=
ENST00000448076.9:c.1200C>T	ENSP00000413452.5:p.Tyr400=
ENST00000452863.10:c.1200C>T MANE Select	ENSP00000415516.5:p.Tyr400=
ENST00000526685.2:n.654C>T
ENST00000639563.3:c.1149C>T	ENSP00000492269.3:p.Tyr383=
ENST00000639907.2:n.343C>T
ENST00000640146.2:c.525C>T	ENSP00000491984.2:p.Tyr175=
ENST00000650861.1:n.1781C>T
ENST00000651459.1:c.36-3566C>T
ENST00000651668.1:n.137C>T
ENST00000651794.1:n.943C>T
ENST00000651819.1:n.125C>T
ENST00000652579.1:n.360C>T
ENST00000652724.1:n.390C>T
ENST00000332351.7:c.1185C>T	ENSP00000331327.3:p.Tyr395=
ENST00000379077.7:c.*384C>T	ENSP00000368368.3:n.*384C>T
ENST00000379079.6:c.549C>T	ENSP00000368370.2:p.Tyr183=
ENST00000448076.7:c.1185C>T	ENSP00000413452.3:p.Tyr395=
ENST00000452863.7:c.1134C>T	ENSP00000415516.3:p.Tyr378=
ENST00000526685.1:c.12C>T	ENSP00000436292.1:p.Tyr4=
ENST00000527882.5:c.256C>T
ENST00000530998.5:c.498C>T	ENSP00000435307.1:p.Tyr166=
NM_000378.4:c.1134C>T	NP_000369.3:p.Tyr378=
NM_001198551.1:c.549C>T , LRG_525t2:c.549C>T	NP_001185480.1:p.Tyr183=
NM_001198552.1:c.498C>T	NP_001185481.1:p.Tyr166=
NM_024424.3:c.1185C>T	NP_077742.2:p.Tyr395=
NM_024426.4:c.1185C>T	NP_077744.3:p.Tyr395=
NM_000378.5:c.1149C>T	NP_000369.4:p.Tyr383=
NM_024424.4:c.1200C>T	NP_077742.3:p.Tyr400=
NM_024426.5:c.1200C>T	NP_077744.4:p.Tyr400=
NM_001367854.1:c.12C>T	NP_001354783.1:p.Tyr4=
NR_160306.1:n.1532C>T
NM_000378.6:c.1149C>T	NP_000369.4:p.Tyr383=
NM_001198552.2:c.498C>T	NP_001185481.1:p.Tyr166=
NM_024424.5:c.1200C>T	NP_077742.3:p.Tyr400=
NM_024426.6:c.1200C>T MANE Select	NP_077744.4:p.Tyr400=