Canonical Allele Identifier: CA379960337

Gene: WT1

Linked Data

• ClinVar Variation Id: 2679626
• ClinVar RCV Id: RCV003464884
• MyVariant Identifiers: chr11:g.32421526T>C (hg19) ; chr11:g.32399980T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32399980T>C , CM000673.2:g.32399980T>C	GRCh38
NC_000011.9:g.32421526T>C , CM000673.1:g.32421526T>C	GRCh37
NC_000011.8:g.32378102T>C	NCBI36
NG_009272.1:g.40562A>G , LRG_525:g.40562A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1030A>G	ENSP00000331327.5:p.Ile344Val
ENST00000379077.9:c.*265A>G	ENSP00000368368.5:n.*265A>G
ENST00000379079.8:c.430A>G	ENSP00000368370.2:p.Ile144Val
ENST00000448076.9:c.1081A>G	ENSP00000413452.5:p.Ile361Val
ENST00000452863.10:c.1081A>G MANE Select	ENSP00000415516.5:p.Ile361Val
ENST00000526685.2:n.535A>G
ENST00000639563.3:c.1030A>G	ENSP00000492269.3:p.Ile344Val
ENST00000639907.2:n.224A>G
ENST00000640146.2:c.406A>G	ENSP00000491984.2:p.Ile136Val
ENST00000651459.1:c.3A>G
ENST00000651794.1:n.824A>G
ENST00000652579.1:n.241A>G
ENST00000652724.1:n.271A>G
ENST00000332351.7:c.1066A>G	ENSP00000331327.3:p.Ile356Val
ENST00000379077.7:c.*265A>G	ENSP00000368368.3:n.*265A>G
ENST00000379079.6:c.430A>G	ENSP00000368370.2:p.Ile144Val
ENST00000448076.7:c.1066A>G	ENSP00000413452.3:p.Ile356Val
ENST00000452863.7:c.1015A>G	ENSP00000415516.3:p.Ile339Val
ENST00000526685.1:c.-108A>G	ENSP00000436292.1:n.-108A>G
ENST00000527775.1:c.319A>G	ENSP00000435351.1:p.Ile107Val
ENST00000527882.5:c.137A>G
ENST00000530998.5:c.379A>G	ENSP00000435307.1:p.Ile127Val
NM_000378.4:c.1015A>G	NP_000369.3:p.Ile339Val
NM_001198551.1:c.430A>G , LRG_525t2:c.430A>G	NP_001185480.1:p.Ile144Val
NM_001198552.1:c.379A>G	NP_001185481.1:p.Ile127Val
NM_024424.3:c.1066A>G	NP_077742.2:p.Ile356Val
NM_024426.4:c.1066A>G	NP_077744.3:p.Ile356Val
NM_000378.5:c.1030A>G	NP_000369.4:p.Ile344Val
NM_024424.4:c.1081A>G	NP_077742.3:p.Ile361Val
NM_024426.5:c.1081A>G	NP_077744.4:p.Ile361Val
NM_001367854.1:c.-108A>G	NP_001354783.1:n.-108A>G
NR_160306.1:n.1413A>G
NM_000378.6:c.1030A>G	NP_000369.4:p.Ile344Val
NM_001198552.2:c.379A>G	NP_001185481.1:p.Ile127Val
NM_024424.5:c.1081A>G	NP_077742.3:p.Ile361Val
NM_024426.6:c.1081A>G MANE Select	NP_077744.4:p.Ile361Val