Canonical Allele Identifier: CA598512818

Gene: WT1

Linked Data

• dbSNP Id: rs1485065050
• gnomAD v2: 11-32456908-A-G
• gnomAD v4: 11-32435362-A-G
• MyVariant Identifiers: chr11:g.32456908A>G (hg19) ; chr11:g.32435362A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32435362A>G , CM000673.2:g.32435362A>G	GRCh38
NC_000011.9:g.32456908A>G , CM000673.1:g.32456908A>G	GRCh37
NC_000011.8:g.32413484A>G	NCBI36
NG_009272.1:g.5180T>C , LRG_525:g.5180T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.-2T>C	ENSP00000331327.5:n.-2T>C
ENST00000379077.9:c.-2T>C	ENSP00000368368.5:n.-2T>C
ENST00000448076.9:c.-2T>C	ENSP00000413452.5:n.-2T>C
ENST00000452863.10:c.-2T>C MANE Select	ENSP00000415516.5:n.-2T>C
ENST00000332351.7:c.-17T>C	ENSP00000331327.3:n.-17T>C
ENST00000379077.7:c.-17T>C	ENSP00000368368.3:n.-17T>C
ENST00000448076.7:c.-17T>C	ENSP00000413452.3:n.-17T>C
NM_000378.4:c.-17T>C	NP_000369.3:n.-17T>C
NM_024424.3:c.-17T>C	NP_077742.2:n.-17T>C
NM_024426.4:c.-17T>C	NP_077744.3:n.-17T>C
NM_000378.5:c.-2T>C	NP_000369.4:n.-2T>C
NM_024424.4:c.-2T>C	NP_077742.3:n.-2T>C
NM_024426.5:c.-2T>C	NP_077744.4:n.-2T>C
NR_160306.1:n.178T>C
NM_000378.6:c.-2T>C	NP_000369.4:n.-2T>C
NM_024424.5:c.-2T>C	NP_077742.3:n.-2T>C
NM_024426.6:c.-2T>C MANE Select	NP_077744.4:n.-2T>C