Canonical Allele Identifier: CA473566980

Gene: WT1

Linked Data

• dbSNP Id: rs1184250193
• gnomAD v2: 11-32417855-A-G
• gnomAD v4: 11-32396309-A-G
• MyVariant Identifiers: chr11:g.32417855A>G (hg19) ; chr11:g.32396309A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32396309A>G , CM000673.2:g.32396309A>G	GRCh38
NC_000011.9:g.32417855A>G , CM000673.1:g.32417855A>G	GRCh37
NC_000011.8:g.32374431A>G	NCBI36
NG_009272.1:g.44233T>C , LRG_525:g.44233T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1161T>C	ENSP00000331327.5:p.Asn387=
ENST00000379077.9:c.*396T>C	ENSP00000368368.5:n.*396T>C
ENST00000379079.8:c.561T>C	ENSP00000368370.2:p.Asn187=
ENST00000448076.9:c.1212T>C	ENSP00000413452.5:p.Asn404=
ENST00000452863.10:c.1212T>C MANE Select	ENSP00000415516.5:p.Asn404=
ENST00000526685.2:n.666T>C
ENST00000639563.3:c.1161T>C	ENSP00000492269.3:p.Asn387=
ENST00000639907.2:n.355T>C
ENST00000640146.2:c.537T>C	ENSP00000491984.2:p.Asn179=
ENST00000650861.1:n.1793T>C
ENST00000651459.1:c.36-3554T>C
ENST00000651668.1:n.149T>C
ENST00000651794.1:n.955T>C
ENST00000651819.1:n.137T>C
ENST00000652579.1:n.372T>C
ENST00000652724.1:n.402T>C
ENST00000332351.7:c.1197T>C	ENSP00000331327.3:p.Asn399=
ENST00000379077.7:c.*396T>C	ENSP00000368368.3:n.*396T>C
ENST00000379079.6:c.561T>C	ENSP00000368370.2:p.Asn187=
ENST00000448076.7:c.1197T>C	ENSP00000413452.3:p.Asn399=
ENST00000452863.7:c.1146T>C	ENSP00000415516.3:p.Asn382=
ENST00000526685.1:c.24T>C	ENSP00000436292.1:p.Asn8=
ENST00000527882.5:c.268T>C
ENST00000530998.5:c.510T>C	ENSP00000435307.1:p.Asn170=
NM_000378.4:c.1146T>C	NP_000369.3:p.Asn382=
NM_001198551.1:c.561T>C , LRG_525t2:c.561T>C	NP_001185480.1:p.Asn187=
NM_001198552.1:c.510T>C	NP_001185481.1:p.Asn170=
NM_024424.3:c.1197T>C	NP_077742.2:p.Asn399=
NM_024426.4:c.1197T>C	NP_077744.3:p.Asn399=
NM_000378.5:c.1161T>C	NP_000369.4:p.Asn387=
NM_024424.4:c.1212T>C	NP_077742.3:p.Asn404=
NM_024426.5:c.1212T>C	NP_077744.4:p.Asn404=
NM_001367854.1:c.24T>C	NP_001354783.1:p.Asn8=
NR_160306.1:n.1544T>C
NM_000378.6:c.1161T>C	NP_000369.4:p.Asn387=
NM_001198552.2:c.510T>C	NP_001185481.1:p.Asn170=
NM_024424.5:c.1212T>C	NP_077742.3:p.Asn404=
NM_024426.6:c.1212T>C MANE Select	NP_077744.4:p.Asn404=