Canonical Allele Identifier: CA379962216

Gene: WT1

Linked Data

• ClinVar Variation Id: 543137
• ClinVar RCV Id: RCV000653800 ; RCV003465415
• dbSNP Id: rs1554943492
• gnomAD v3: 11-32417650-T-C
• gnomAD v4: 11-32417650-T-C
• MyVariant Identifiers: chr11:g.32439196T>C (hg19) ; chr11:g.32417650T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32417650T>C , CM000673.2:g.32417650T>C	GRCh38
NC_000011.9:g.32439196T>C , CM000673.1:g.32439196T>C	GRCh37
NC_000011.8:g.32395772T>C	NCBI36
NG_009272.1:g.22892A>G , LRG_525:g.22892A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.892A>G	ENSP00000331327.5:p.Asn298Asp
ENST00000379077.9:c.892A>G	ENSP00000368368.5:p.Asn298Asp
ENST00000379079.8:c.241A>G	ENSP00000368370.2:p.Asn81Asp
ENST00000448076.9:c.892A>G	ENSP00000413452.5:p.Asn298Asp
ENST00000452863.10:c.892A>G MANE Select	ENSP00000415516.5:p.Asn298Asp
ENST00000639563.3:c.892A>G	ENSP00000492269.3:p.Asn298Asp
ENST00000640146.2:c.268A>G	ENSP00000491984.2:p.Asn90Asp
ENST00000332351.7:c.877A>G	ENSP00000331327.3:p.Asn293Asp
ENST00000379077.7:c.877A>G	ENSP00000368368.3:p.Asn293Asp
ENST00000379079.6:c.241A>G	ENSP00000368370.2:p.Asn81Asp
ENST00000448076.7:c.877A>G	ENSP00000413452.3:p.Asn293Asp
ENST00000452863.7:c.877A>G	ENSP00000415516.3:p.Asn293Asp
ENST00000527775.1:c.130A>G	ENSP00000435351.1:p.Asn44Asp
ENST00000530998.5:c.241A>G	ENSP00000435307.1:p.Asn81Asp
NM_000378.4:c.877A>G	NP_000369.3:p.Asn293Asp
NM_001198551.1:c.241A>G , LRG_525t2:c.241A>G	NP_001185480.1:p.Asn81Asp
NM_001198552.1:c.241A>G	NP_001185481.1:p.Asn81Asp
NM_024424.3:c.877A>G	NP_077742.2:p.Asn293Asp
NM_024426.4:c.877A>G	NP_077744.3:p.Asn293Asp
NM_000378.5:c.892A>G	NP_000369.4:p.Asn298Asp
NM_024424.4:c.892A>G	NP_077742.3:p.Asn298Asp
NM_024426.5:c.892A>G	NP_077744.4:p.Asn298Asp
NR_160306.1:n.1071A>G
NM_000378.6:c.892A>G	NP_000369.4:p.Asn298Asp
NM_001198552.2:c.241A>G	NP_001185481.1:p.Asn81Asp
NM_024424.5:c.892A>G	NP_077742.3:p.Asn298Asp
NM_024426.6:c.892A>G MANE Select	NP_077744.4:p.Asn298Asp