Canonical Allele Identifier: CA473566936

Gene: WT1

Linked Data

• dbSNP Id: rs1851967619
• MyVariant Identifiers: chr11:g.32417846A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32396300A>G , CM000673.2:g.32396300A>G	GRCh38
NC_000011.9:g.32417846A>G , CM000673.1:g.32417846A>G	GRCh37
NC_000011.8:g.32374422A>G	NCBI36
NG_009272.1:g.44242T>C , LRG_525:g.44242T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1170T>C	ENSP00000331327.5:p.Tyr390=
ENST00000379077.9:c.*405T>C	ENSP00000368368.5:n.*405T>C
ENST00000379079.8:c.570T>C	ENSP00000368370.2:p.Tyr190=
ENST00000448076.9:c.1221T>C	ENSP00000413452.5:p.Tyr407=
ENST00000452863.10:c.1221T>C MANE Select	ENSP00000415516.5:p.Tyr407=
ENST00000526685.2:n.675T>C
ENST00000639563.3:c.1170T>C	ENSP00000492269.3:p.Tyr390=
ENST00000639907.2:n.364T>C
ENST00000640146.2:c.546T>C	ENSP00000491984.2:p.Tyr182=
ENST00000650861.1:n.1802T>C
ENST00000651459.1:c.36-3545T>C
ENST00000651668.1:n.158T>C
ENST00000651794.1:n.964T>C
ENST00000651819.1:n.146T>C
ENST00000652579.1:n.381T>C
ENST00000652724.1:n.411T>C
ENST00000332351.7:c.1206T>C	ENSP00000331327.3:p.Tyr402=
ENST00000379077.7:c.*405T>C	ENSP00000368368.3:n.*405T>C
ENST00000379079.6:c.570T>C	ENSP00000368370.2:p.Tyr190=
ENST00000448076.7:c.1206T>C	ENSP00000413452.3:p.Tyr402=
ENST00000452863.7:c.1155T>C	ENSP00000415516.3:p.Tyr385=
ENST00000526685.1:c.33T>C	ENSP00000436292.1:p.Tyr11=
ENST00000527882.5:c.277T>C
ENST00000530998.5:c.519T>C	ENSP00000435307.1:p.Tyr173=
NM_000378.4:c.1155T>C	NP_000369.3:p.Tyr385=
NM_001198551.1:c.570T>C , LRG_525t2:c.570T>C	NP_001185480.1:p.Tyr190=
NM_001198552.1:c.519T>C	NP_001185481.1:p.Tyr173=
NM_024424.3:c.1206T>C	NP_077742.2:p.Tyr402=
NM_024426.4:c.1206T>C	NP_077744.3:p.Tyr402=
NM_000378.5:c.1170T>C	NP_000369.4:p.Tyr390=
NM_024424.4:c.1221T>C	NP_077742.3:p.Tyr407=
NM_024426.5:c.1221T>C	NP_077744.4:p.Tyr407=
NM_001367854.1:c.33T>C	NP_001354783.1:p.Tyr11=
NR_160306.1:n.1553T>C
NM_000378.6:c.1170T>C	NP_000369.4:p.Tyr390=
NM_001198552.2:c.519T>C	NP_001185481.1:p.Tyr173=
NM_024424.5:c.1221T>C	NP_077742.3:p.Tyr407=
NM_024426.6:c.1221T>C MANE Select	NP_077744.4:p.Tyr407=