Canonical Allele Identifier: CA473567323

Gene: WT1

Linked Data

• dbSNP Id: rs17855567
• MyVariant Identifiers: chr11:g.32421524T>G (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1032A>C	ENSP00000331327.5:p.Ile344=
ENST00000379077.9:c.*267A>C	ENSP00000368368.5:n.*267A>C
ENST00000379079.8:c.432A>C	ENSP00000368370.2:p.Ile144=
ENST00000448076.9:c.1083A>C	ENSP00000413452.5:p.Ile361=
ENST00000452863.10:c.1083A>C MANE Select	ENSP00000415516.5:p.Ile361=
ENST00000526685.2:n.537A>C
ENST00000639563.3:c.1032A>C	ENSP00000492269.3:p.Ile344=
ENST00000639907.2:n.226A>C
ENST00000640146.2:c.408A>C	ENSP00000491984.2:p.Ile136=
ENST00000651459.1:c.5A>C
ENST00000651794.1:n.826A>C
ENST00000652579.1:n.243A>C
ENST00000652724.1:n.273A>C
ENST00000332351.7:c.1068A>C	ENSP00000331327.3:p.Ile356=
ENST00000379077.7:c.*267A>C	ENSP00000368368.3:n.*267A>C
ENST00000379079.6:c.432A>C	ENSP00000368370.2:p.Ile144=
ENST00000448076.7:c.1068A>C	ENSP00000413452.3:p.Ile356=
ENST00000452863.7:c.1017A>C	ENSP00000415516.3:p.Ile339=
ENST00000526685.1:c.-106A>C	ENSP00000436292.1:n.-106A>C
ENST00000527775.1:c.321A>C	ENSP00000435351.1:p.Ile107=
ENST00000527882.5:c.139A>C
ENST00000530998.5:c.381A>C	ENSP00000435307.1:p.Ile127=
NM_000378.4:c.1017A>C	NP_000369.3:p.Ile339=
NM_001198551.1:c.432A>C , LRG_525t2:c.432A>C	NP_001185480.1:p.Ile144=
NM_001198552.1:c.381A>C	NP_001185481.1:p.Ile127=
NM_024424.3:c.1068A>C	NP_077742.2:p.Ile356=
NM_024426.4:c.1068A>C	NP_077744.3:p.Ile356=
NM_000378.5:c.1032A>C	NP_000369.4:p.Ile344=
NM_024424.4:c.1083A>C	NP_077742.3:p.Ile361=
NM_024426.5:c.1083A>C	NP_077744.4:p.Ile361=
NM_001367854.1:c.-106A>C	NP_001354783.1:n.-106A>C
NR_160306.1:n.1415A>C
NM_000378.6:c.1032A>C	NP_000369.4:p.Ile344=
NM_001198552.2:c.381A>C	NP_001185481.1:p.Ile127=
NM_024424.5:c.1083A>C	NP_077742.3:p.Ile361=
NM_024426.6:c.1083A>C MANE Select	NP_077744.4:p.Ile361=