Canonical Allele Identifier: CA598512821

Gene: WT1

Linked Data

• dbSNP Id: rs1470338786
• gnomAD v2: 11-32456912-C-T
• gnomAD v4: 11-32435366-C-T
• MyVariant Identifiers: chr11:g.32456912C>T (hg19) ; chr11:g.32435366C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32435366C>T , CM000673.2:g.32435366C>T	GRCh38
NC_000011.9:g.32456912C>T , CM000673.1:g.32456912C>T	GRCh37
NC_000011.8:g.32413488C>T	NCBI36
NG_009272.1:g.5176G>A , LRG_525:g.5176G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.-6G>A	ENSP00000331327.5:n.-6G>A
ENST00000379077.9:c.-6G>A	ENSP00000368368.5:n.-6G>A
ENST00000448076.9:c.-6G>A	ENSP00000413452.5:n.-6G>A
ENST00000452863.10:c.-6G>A MANE Select	ENSP00000415516.5:n.-6G>A
ENST00000332351.7:c.-21G>A	ENSP00000331327.3:n.-21G>A
ENST00000379077.7:c.-21G>A	ENSP00000368368.3:n.-21G>A
ENST00000448076.7:c.-21G>A	ENSP00000413452.3:n.-21G>A
NM_000378.4:c.-21G>A	NP_000369.3:n.-21G>A
NM_024424.3:c.-21G>A	NP_077742.2:n.-21G>A
NM_024426.4:c.-21G>A	NP_077744.3:n.-21G>A
NM_000378.5:c.-6G>A	NP_000369.4:n.-6G>A
NM_024424.4:c.-6G>A	NP_077742.3:n.-6G>A
NM_024426.5:c.-6G>A	NP_077744.4:n.-6G>A
NR_160306.1:n.174G>A
NM_000378.6:c.-6G>A	NP_000369.4:n.-6G>A
NM_024424.5:c.-6G>A	NP_077742.3:n.-6G>A
NM_024426.6:c.-6G>A MANE Select	NP_077744.4:n.-6G>A