Canonical Allele Identifier: CA219479420

Gene: WT1

Linked Data

• dbSNP Id: rs17855567
• gnomAD v3: 11-32399978-T-C
• gnomAD v4: 11-32399978-T-C
• MyVariant Identifiers: chr11:g.32421524T>C (hg19) ; chr11:g.32399978T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32399978T>C , CM000673.2:g.32399978T>C	GRCh38
NC_000011.9:g.32421524T>C , CM000673.1:g.32421524T>C	GRCh37
NC_000011.8:g.32378100T>C	NCBI36
NG_009272.1:g.40564A>G , LRG_525:g.40564A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1032A>G	ENSP00000331327.5:p.Ile344Met
ENST00000379077.9:c.*267A>G	ENSP00000368368.5:n.*267A>G
ENST00000379079.8:c.432A>G	ENSP00000368370.2:p.Ile144Met
ENST00000448076.9:c.1083A>G	ENSP00000413452.5:p.Ile361Met
ENST00000452863.10:c.1083A>G MANE Select	ENSP00000415516.5:p.Ile361Met
ENST00000526685.2:n.537A>G
ENST00000639563.3:c.1032A>G	ENSP00000492269.3:p.Ile344Met
ENST00000639907.2:n.226A>G
ENST00000640146.2:c.408A>G	ENSP00000491984.2:p.Ile136Met
ENST00000651459.1:c.5A>G
ENST00000651794.1:n.826A>G
ENST00000652579.1:n.243A>G
ENST00000652724.1:n.273A>G
ENST00000332351.7:c.1068A>G	ENSP00000331327.3:p.Ile356Met
ENST00000379077.7:c.*267A>G	ENSP00000368368.3:n.*267A>G
ENST00000379079.6:c.432A>G	ENSP00000368370.2:p.Ile144Met
ENST00000448076.7:c.1068A>G	ENSP00000413452.3:p.Ile356Met
ENST00000452863.7:c.1017A>G	ENSP00000415516.3:p.Ile339Met
ENST00000526685.1:c.-106A>G	ENSP00000436292.1:n.-106A>G
ENST00000527775.1:c.321A>G	ENSP00000435351.1:p.Ile107Met
ENST00000527882.5:c.139A>G
ENST00000530998.5:c.381A>G	ENSP00000435307.1:p.Ile127Met
NM_000378.4:c.1017A>G	NP_000369.3:p.Ile339Met
NM_001198551.1:c.432A>G , LRG_525t2:c.432A>G	NP_001185480.1:p.Ile144Met
NM_001198552.1:c.381A>G	NP_001185481.1:p.Ile127Met
NM_024424.3:c.1068A>G	NP_077742.2:p.Ile356Met
NM_024426.4:c.1068A>G	NP_077744.3:p.Ile356Met
NM_000378.5:c.1032A>G	NP_000369.4:p.Ile344Met
NM_024424.4:c.1083A>G	NP_077742.3:p.Ile361Met
NM_024426.5:c.1083A>G	NP_077744.4:p.Ile361Met
NM_001367854.1:c.-106A>G	NP_001354783.1:n.-106A>G
NR_160306.1:n.1415A>G
NM_000378.6:c.1032A>G	NP_000369.4:p.Ile344Met
NM_001198552.2:c.381A>G	NP_001185481.1:p.Ile127Met
NM_024424.5:c.1083A>G	NP_077742.3:p.Ile361Met
NM_024426.6:c.1083A>G MANE Select	NP_077744.4:p.Ile361Met