Canonical Allele Identifier: CA598512824

Gene: WT1

Linked Data

• dbSNP Id: rs1436301511
• gnomAD v2: 11-32456928-G-T
• gnomAD v4: 11-32435382-G-T
• MyVariant Identifiers: chr11:g.32456928G>T (hg19) ; chr11:g.32435382G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32435382G>T , CM000673.2:g.32435382G>T	GRCh38
NC_000011.9:g.32456928G>T , CM000673.1:g.32456928G>T	GRCh37
NC_000011.8:g.32413504G>T	NCBI36
NG_009272.1:g.5160C>A , LRG_525:g.5160C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.-22C>A	ENSP00000331327.5:n.-22C>A
ENST00000379077.9:c.-22C>A	ENSP00000368368.5:n.-22C>A
ENST00000448076.9:c.-22C>A	ENSP00000413452.5:n.-22C>A
ENST00000452863.10:c.-22C>A MANE Select	ENSP00000415516.5:n.-22C>A
ENST00000332351.7:c.-37C>A	ENSP00000331327.3:n.-37C>A
ENST00000379077.7:c.-37C>A	ENSP00000368368.3:n.-37C>A
ENST00000448076.7:c.-37C>A	ENSP00000413452.3:n.-37C>A
NM_000378.4:c.-37C>A	NP_000369.3:n.-37C>A
NM_024424.3:c.-37C>A	NP_077742.2:n.-37C>A
NM_024426.4:c.-37C>A	NP_077744.3:n.-37C>A
NM_000378.5:c.-22C>A	NP_000369.4:n.-22C>A
NM_024424.4:c.-22C>A	NP_077742.3:n.-22C>A
NM_024426.5:c.-22C>A	NP_077744.4:n.-22C>A
NR_160306.1:n.158C>A
NM_000378.6:c.-22C>A	NP_000369.4:n.-22C>A
NM_024424.5:c.-22C>A	NP_077742.3:n.-22C>A
NM_024426.6:c.-22C>A MANE Select	NP_077744.4:n.-22C>A