Canonical Allele Identifier: CA379960334

Gene: WT1

Linked Data

• ClinVar Variation Id: 1484902
• ClinVar RCV Id: RCV002030271
• dbSNP Id: rs2132957665
• MyVariant Identifiers: chr11:g.32421525A>G (hg19) ; chr11:g.32399979A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32399979A>G , CM000673.2:g.32399979A>G	GRCh38
NC_000011.9:g.32421525A>G , CM000673.1:g.32421525A>G	GRCh37
NC_000011.8:g.32378101A>G	NCBI36
NG_009272.1:g.40563T>C , LRG_525:g.40563T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1031T>C	ENSP00000331327.5:p.Ile344Thr
ENST00000379077.9:c.*266T>C	ENSP00000368368.5:n.*266T>C
ENST00000379079.8:c.431T>C	ENSP00000368370.2:p.Ile144Thr
ENST00000448076.9:c.1082T>C	ENSP00000413452.5:p.Ile361Thr
ENST00000452863.10:c.1082T>C MANE Select	ENSP00000415516.5:p.Ile361Thr
ENST00000526685.2:n.536T>C
ENST00000639563.3:c.1031T>C	ENSP00000492269.3:p.Ile344Thr
ENST00000639907.2:n.225T>C
ENST00000640146.2:c.407T>C	ENSP00000491984.2:p.Ile136Thr
ENST00000651459.1:c.4T>C
ENST00000651794.1:n.825T>C
ENST00000652579.1:n.242T>C
ENST00000652724.1:n.272T>C
ENST00000332351.7:c.1067T>C	ENSP00000331327.3:p.Ile356Thr
ENST00000379077.7:c.*266T>C	ENSP00000368368.3:n.*266T>C
ENST00000379079.6:c.431T>C	ENSP00000368370.2:p.Ile144Thr
ENST00000448076.7:c.1067T>C	ENSP00000413452.3:p.Ile356Thr
ENST00000452863.7:c.1016T>C	ENSP00000415516.3:p.Ile339Thr
ENST00000526685.1:c.-107T>C	ENSP00000436292.1:n.-107T>C
ENST00000527775.1:c.320T>C	ENSP00000435351.1:p.Ile107Thr
ENST00000527882.5:c.138T>C
ENST00000530998.5:c.380T>C	ENSP00000435307.1:p.Ile127Thr
NM_000378.4:c.1016T>C	NP_000369.3:p.Ile339Thr
NM_001198551.1:c.431T>C , LRG_525t2:c.431T>C	NP_001185480.1:p.Ile144Thr
NM_001198552.1:c.380T>C	NP_001185481.1:p.Ile127Thr
NM_024424.3:c.1067T>C	NP_077742.2:p.Ile356Thr
NM_024426.4:c.1067T>C	NP_077744.3:p.Ile356Thr
NM_000378.5:c.1031T>C	NP_000369.4:p.Ile344Thr
NM_024424.4:c.1082T>C	NP_077742.3:p.Ile361Thr
NM_024426.5:c.1082T>C	NP_077744.4:p.Ile361Thr
NM_001367854.1:c.-107T>C	NP_001354783.1:n.-107T>C
NR_160306.1:n.1414T>C
NM_000378.6:c.1031T>C	NP_000369.4:p.Ile344Thr
NM_001198552.2:c.380T>C	NP_001185481.1:p.Ile127Thr
NM_024424.5:c.1082T>C	NP_077742.3:p.Ile361Thr
NM_024426.6:c.1082T>C MANE Select	NP_077744.4:p.Ile361Thr