Canonical Allele Identifier: CA065416

Gene: WT1

Linked Data

• ClinVar Variation Id: 241486
• ClinVar RCV Id: RCV000227539 ; RCV000455551 ; RCV000988517 ; RCV001567721 ; RCV002256171
• dbSNP Id: rs372418954
• ExAC: 11:32450171 G / T
• gnomAD v2: 11-32450171-G-T
• gnomAD v3: 11-32428625-G-T
• gnomAD v4: 11-32428625-G-T
• COSMIC: COSM4167578 ; COSM4167579 ; COSM4167580
• MyVariant Identifiers: chr11:g.32450171G>T (hg19) ; chr11:g.32428625G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32428625G>T , CM000673.2:g.32428625G>T	GRCh38
NC_000011.9:g.32450171G>T , CM000673.1:g.32450171G>T	GRCh37
NC_000011.8:g.32406747G>T	NCBI36
NG_009272.1:g.11917C>A , LRG_525:g.11917C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.662-6C>A	ENSP00000331327.5:n.662-6C>A
ENST00000379077.9:c.662-6C>A	ENSP00000368368.5:n.662-6C>A
ENST00000379079.8:c.11-6C>A	ENSP00000368370.2:n.11-6C>A
ENST00000448076.9:c.662-6C>A	ENSP00000413452.5:n.662-6C>A
ENST00000452863.10:c.662-6C>A MANE Select	ENSP00000415516.5:n.662-6C>A
ENST00000639563.3:c.662-6C>A	ENSP00000492269.3:n.662-6C>A
ENST00000640146.2:c.38-6C>A	ENSP00000491984.2:n.38-6C>A
ENST00000332351.7:c.647-6C>A	ENSP00000331327.3:n.647-6C>A
ENST00000379077.7:c.647-6C>A	ENSP00000368368.3:n.647-6C>A
ENST00000379079.6:c.11-6C>A	ENSP00000368370.2:n.11-6C>A
ENST00000448076.7:c.647-6C>A	ENSP00000413452.3:n.647-6C>A
ENST00000452863.7:c.647-6C>A	ENSP00000415516.3:n.647-6C>A
ENST00000527775.1:c.-101-6C>A	ENSP00000435351.1:n.-101-6C>A
ENST00000530998.5:c.11-6C>A	ENSP00000435307.1:n.11-6C>A
NM_000378.4:c.647-6C>A	NP_000369.3:n.647-6C>A
NM_001198551.1:c.11-6C>A , LRG_525t2:c.11-6C>A	NP_001185480.1:n.11-6C>A
NM_001198552.1:c.11-6C>A	NP_001185481.1:n.11-6C>A
NM_024424.3:c.647-6C>A	NP_077742.2:n.647-6C>A
NM_024426.4:c.647-6C>A	NP_077744.3:n.647-6C>A
NM_000378.5:c.662-6C>A	NP_000369.4:n.662-6C>A
NM_024424.4:c.662-6C>A	NP_077742.3:n.662-6C>A
NM_024426.5:c.662-6C>A	NP_077744.4:n.662-6C>A
NR_160306.1:n.841-6C>A
NM_000378.6:c.662-6C>A	NP_000369.4:n.662-6C>A
NM_001198552.2:c.11-6C>A	NP_001185481.1:n.11-6C>A
NM_024424.5:c.662-6C>A	NP_077742.3:n.662-6C>A
NM_024426.6:c.662-6C>A MANE Select	NP_077744.4:n.662-6C>A