Canonical Allele Identifier: CA065807

Gene: WT1

Linked Data

• ClinVar Variation Id: 304421
• ClinVar RCV Id: RCV000261951 ; RCV000353359 ; RCV000368224 ; RCV000470103
• dbSNP Id: rs778673400
• ExAC: 11:32449498 C / T
• gnomAD v2: 11-32449498-C-T
• gnomAD v3: 11-32427952-C-T
• gnomAD v4: 11-32427952-C-T
• MyVariant Identifiers: chr11:g.32449498C>T (hg19) ; chr11:g.32427952C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32427952C>T , CM000673.2:g.32427952C>T	GRCh38
NC_000011.9:g.32449498C>T , CM000673.1:g.32449498C>T	GRCh37
NC_000011.8:g.32406074C>T	NCBI36
NG_009272.1:g.12590G>A , LRG_525:g.12590G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.887+4G>A	ENSP00000331327.5:n.887+4G>A
ENST00000379077.9:c.887+4G>A	ENSP00000368368.5:n.887+4G>A
ENST00000379079.8:c.236+4G>A	ENSP00000368370.2:n.236+4G>A
ENST00000448076.9:c.887+4G>A	ENSP00000413452.5:n.887+4G>A
ENST00000452863.10:c.887+4G>A MANE Select	ENSP00000415516.5:n.887+4G>A
ENST00000639563.3:c.887+4G>A	ENSP00000492269.3:n.887+4G>A
ENST00000640146.2:c.263+4G>A	ENSP00000491984.2:n.263+4G>A
ENST00000332351.7:c.872+4G>A	ENSP00000331327.3:n.872+4G>A
ENST00000379077.7:c.872+4G>A	ENSP00000368368.3:n.872+4G>A
ENST00000379079.6:c.236+4G>A	ENSP00000368370.2:n.236+4G>A
ENST00000448076.7:c.872+4G>A	ENSP00000413452.3:n.872+4G>A
ENST00000452863.7:c.872+4G>A	ENSP00000415516.3:n.872+4G>A
ENST00000527775.1:c.125+4G>A	ENSP00000435351.1:n.125+4G>A
ENST00000530998.5:c.236+4G>A	ENSP00000435307.1:n.236+4G>A
NM_000378.4:c.872+4G>A	NP_000369.3:n.872+4G>A
NM_001198551.1:c.236+4G>A , LRG_525t2:c.236+4G>A	NP_001185480.1:n.236+4G>A
NM_001198552.1:c.236+4G>A	NP_001185481.1:n.236+4G>A
NM_024424.3:c.872+4G>A	NP_077742.2:n.872+4G>A
NM_024426.4:c.872+4G>A	NP_077744.3:n.872+4G>A
NM_000378.5:c.887+4G>A	NP_000369.4:n.887+4G>A
NM_024424.4:c.887+4G>A	NP_077742.3:n.887+4G>A
NM_024426.5:c.887+4G>A	NP_077744.4:n.887+4G>A
NR_160306.1:n.1066+4G>A
NM_000378.6:c.887+4G>A	NP_000369.4:n.887+4G>A
NM_001198552.2:c.236+4G>A	NP_001185481.1:n.236+4G>A
NM_024424.5:c.887+4G>A	NP_077742.3:n.887+4G>A
NM_024426.6:c.887+4G>A MANE Select	NP_077744.4:n.887+4G>A