Canonical Allele Identifier: CA379963268

Gene: WT1

Linked Data

• dbSNP Id: rs1352932484
• gnomAD v2: 11-32450052-C-A
• gnomAD v4: 11-32428506-C-A
• MyVariant Identifiers: chr11:g.32450052C>A (hg19) ; chr11:g.32428506C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32428506C>A , CM000673.2:g.32428506C>A	GRCh38
NC_000011.9:g.32450052C>A , CM000673.1:g.32450052C>A	GRCh37
NC_000011.8:g.32406628C>A	NCBI36
NG_009272.1:g.12036G>T , LRG_525:g.12036G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.775G>T	ENSP00000331327.5:p.Gly259Cys
ENST00000379077.9:c.775G>T	ENSP00000368368.5:p.Gly259Cys
ENST00000379079.8:c.124G>T	ENSP00000368370.2:p.Gly42Cys
ENST00000448076.9:c.775G>T	ENSP00000413452.5:p.Gly259Cys
ENST00000452863.10:c.775G>T MANE Select	ENSP00000415516.5:p.Gly259Cys
ENST00000639563.3:c.775G>T	ENSP00000492269.3:p.Gly259Cys
ENST00000640146.2:c.151G>T	ENSP00000491984.2:p.Gly51Cys
ENST00000332351.7:c.760G>T	ENSP00000331327.3:p.Gly254Cys
ENST00000379077.7:c.760G>T	ENSP00000368368.3:p.Gly254Cys
ENST00000379079.6:c.124G>T	ENSP00000368370.2:p.Gly42Cys
ENST00000448076.7:c.760G>T	ENSP00000413452.3:p.Gly254Cys
ENST00000452863.7:c.760G>T	ENSP00000415516.3:p.Gly254Cys
ENST00000527775.1:c.13G>T	ENSP00000435351.1:p.Gly5Cys
ENST00000530998.5:c.124G>T	ENSP00000435307.1:p.Gly42Cys
NM_000378.4:c.760G>T	NP_000369.3:p.Gly254Cys
NM_001198551.1:c.124G>T , LRG_525t2:c.124G>T	NP_001185480.1:p.Gly42Cys
NM_001198552.1:c.124G>T	NP_001185481.1:p.Gly42Cys
NM_024424.3:c.760G>T	NP_077742.2:p.Gly254Cys
NM_024426.4:c.760G>T	NP_077744.3:p.Gly254Cys
NM_000378.5:c.775G>T	NP_000369.4:p.Gly259Cys
NM_024424.4:c.775G>T	NP_077742.3:p.Gly259Cys
NM_024426.5:c.775G>T	NP_077744.4:p.Gly259Cys
NR_160306.1:n.954G>T
NM_000378.6:c.775G>T	NP_000369.4:p.Gly259Cys
NM_001198552.2:c.124G>T	NP_001185481.1:p.Gly42Cys
NM_024424.5:c.775G>T	NP_077742.3:p.Gly259Cys
NM_024426.6:c.775G>T MANE Select	NP_077744.4:p.Gly259Cys