Canonical Allele Identifier: CA473565889

Gene: WT1

Linked Data

• dbSNP Id: rs2132920912
• gnomAD v4: 11-32392724-G-A
• MyVariant Identifiers: chr11:g.32414270G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392724G>A , CM000673.2:g.32392724G>A	GRCh38
NC_000011.9:g.32414270G>A , CM000673.1:g.32414270G>A	GRCh37
NC_000011.8:g.32370846G>A	NCBI36
NG_009272.1:g.47818C>T , LRG_525:g.47818C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1245C>T	ENSP00000331327.5:p.Asp415=
ENST00000379077.9:c.*480C>T	ENSP00000368368.5:n.*480C>T
ENST00000379079.8:c.645C>T	ENSP00000368370.2:p.Asp215=
ENST00000448076.9:c.1296C>T	ENSP00000413452.5:p.Asp432=
ENST00000452863.10:c.1296C>T MANE Select	ENSP00000415516.5:p.Asp432=
ENST00000526685.2:n.750C>T
ENST00000639563.3:c.1245C>T	ENSP00000492269.3:p.Asp415=
ENST00000639907.2:n.439C>T
ENST00000640146.2:c.621C>T	ENSP00000491984.2:p.Asp207=
ENST00000650745.1:n.505C>T
ENST00000650861.1:n.1877C>T
ENST00000651459.1:c.67C>T
ENST00000651533.1:n.342C>T
ENST00000651668.1:n.233C>T
ENST00000651794.1:n.1139C>T
ENST00000651819.1:n.221C>T
ENST00000652579.1:n.556C>T
ENST00000652724.1:n.486C>T
ENST00000332351.7:c.1281C>T	ENSP00000331327.3:p.Asp427=
ENST00000379077.7:c.*480C>T	ENSP00000368368.3:n.*480C>T
ENST00000379079.6:c.645C>T	ENSP00000368370.2:p.Asp215=
ENST00000448076.7:c.1281C>T	ENSP00000413452.3:p.Asp427=
ENST00000452863.7:c.1230C>T	ENSP00000415516.3:p.Asp410=
ENST00000527882.5:c.321-660C>T
ENST00000530998.5:c.594C>T	ENSP00000435307.1:p.Asp198=
NM_000378.4:c.1230C>T	NP_000369.3:p.Asp410=
NM_001198551.1:c.645C>T , LRG_525t2:c.645C>T	NP_001185480.1:p.Asp215=
NM_001198552.1:c.594C>T	NP_001185481.1:p.Asp198=
NM_024424.3:c.1281C>T	NP_077742.2:p.Asp427=
NM_024426.4:c.1281C>T	NP_077744.3:p.Asp427=
NM_000378.5:c.1245C>T	NP_000369.4:p.Asp415=
NM_024424.4:c.1296C>T	NP_077742.3:p.Asp432=
NM_024426.5:c.1296C>T	NP_077744.4:p.Asp432=
NM_001367854.1:c.108C>T	NP_001354783.1:p.Asp36=
NR_160306.1:n.1628C>T
NM_000378.6:c.1245C>T	NP_000369.4:p.Asp415=
NM_001198552.2:c.594C>T	NP_001185481.1:p.Asp198=
NM_024424.5:c.1296C>T	NP_077742.3:p.Asp432=
NM_024426.6:c.1296C>T MANE Select	NP_077744.4:p.Asp432=