Canonical Allele Identifier: CA473567316

Gene: WT1

Linked Data

• ClinVar Variation Id: 1117183
• ClinVar RCV Id: RCV001445844
• dbSNP Id: rs587778756
• gnomAD v2: 11-32421515-G-A
• gnomAD v4: 11-32399969-G-A
• MyVariant Identifiers: chr11:g.32421515G>A (hg19) ; chr11:g.32399969G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32399969G>A , CM000673.2:g.32399969G>A	GRCh38
NC_000011.9:g.32421515G>A , CM000673.1:g.32421515G>A	GRCh37
NC_000011.8:g.32378091G>A	NCBI36
NG_009272.1:g.40573C>T , LRG_525:g.40573C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1041C>T	ENSP00000331327.5:p.His347=
ENST00000379077.9:c.*276C>T	ENSP00000368368.5:n.*276C>T
ENST00000379079.8:c.441C>T	ENSP00000368370.2:p.His147=
ENST00000448076.9:c.1092C>T	ENSP00000413452.5:p.His364=
ENST00000452863.10:c.1092C>T MANE Select	ENSP00000415516.5:p.His364=
ENST00000526685.2:n.546C>T
ENST00000639563.3:c.1041C>T	ENSP00000492269.3:p.His347=
ENST00000639907.2:n.235C>T
ENST00000640146.2:c.417C>T	ENSP00000491984.2:p.His139=
ENST00000651459.1:c.14C>T
ENST00000651794.1:n.835C>T
ENST00000652579.1:n.252C>T
ENST00000652724.1:n.282C>T
ENST00000332351.7:c.1077C>T	ENSP00000331327.3:p.His359=
ENST00000379077.7:c.*276C>T	ENSP00000368368.3:n.*276C>T
ENST00000379079.6:c.441C>T	ENSP00000368370.2:p.His147=
ENST00000448076.7:c.1077C>T	ENSP00000413452.3:p.His359=
ENST00000452863.7:c.1026C>T	ENSP00000415516.3:p.His342=
ENST00000526685.1:c.-97C>T	ENSP00000436292.1:n.-97C>T
ENST00000527775.1:c.330C>T	ENSP00000435351.1:p.His110=
ENST00000527882.5:c.148C>T
ENST00000530998.5:c.390C>T	ENSP00000435307.1:p.His130=
NM_000378.4:c.1026C>T	NP_000369.3:p.His342=
NM_001198551.1:c.441C>T , LRG_525t2:c.441C>T	NP_001185480.1:p.His147=
NM_001198552.1:c.390C>T	NP_001185481.1:p.His130=
NM_024424.3:c.1077C>T	NP_077742.2:p.His359=
NM_024426.4:c.1077C>T	NP_077744.3:p.His359=
NM_000378.5:c.1041C>T	NP_000369.4:p.His347=
NM_024424.4:c.1092C>T	NP_077742.3:p.His364=
NM_024426.5:c.1092C>T	NP_077744.4:p.His364=
NM_001367854.1:c.-97C>T	NP_001354783.1:n.-97C>T
NR_160306.1:n.1424C>T
NM_000378.6:c.1041C>T	NP_000369.4:p.His347=
NM_001198552.2:c.390C>T	NP_001185481.1:p.His130=
NM_024424.5:c.1092C>T	NP_077742.3:p.His364=
NM_024426.6:c.1092C>T MANE Select	NP_077744.4:p.His364=