Canonical Allele Identifier: CA379959980

Gene: WT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32396350T>G , CM000673.2:g.32396350T>G	GRCh38
NC_000011.9:g.32417896T>G , CM000673.1:g.32417896T>G	GRCh37
NC_000011.8:g.32374472T>G	NCBI36
NG_009272.1:g.44192A>C , LRG_525:g.44192A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1120A>C	ENSP00000331327.5:p.Ser374Arg
ENST00000379077.9:c.*355A>C	ENSP00000368368.5:n.*355A>C
ENST00000379079.8:c.520A>C	ENSP00000368370.2:p.Ser174Arg
ENST00000448076.9:c.1171A>C	ENSP00000413452.5:p.Ser391Arg
ENST00000452863.10:c.1171A>C MANE Select	ENSP00000415516.5:p.Ser391Arg
ENST00000526685.2:n.625A>C
ENST00000639563.3:c.1120A>C	ENSP00000492269.3:p.Ser374Arg
ENST00000639907.2:n.314A>C
ENST00000640146.2:c.496A>C	ENSP00000491984.2:p.Ser166Arg
ENST00000650861.1:n.1752A>C
ENST00000651459.1:c.36-3595A>C
ENST00000651668.1:n.108A>C
ENST00000651794.1:n.914A>C
ENST00000651819.1:n.96A>C
ENST00000652579.1:n.331A>C
ENST00000652724.1:n.361A>C
ENST00000332351.7:c.1156A>C	ENSP00000331327.3:p.Ser386Arg
ENST00000379077.7:c.*355A>C	ENSP00000368368.3:n.*355A>C
ENST00000379079.6:c.520A>C	ENSP00000368370.2:p.Ser174Arg
ENST00000448076.7:c.1156A>C	ENSP00000413452.3:p.Ser386Arg
ENST00000452863.7:c.1105A>C	ENSP00000415516.3:p.Ser369Arg
ENST00000526685.1:c.-18A>C	ENSP00000436292.1:n.-18A>C
ENST00000527882.5:c.227A>C
ENST00000530998.5:c.469A>C	ENSP00000435307.1:p.Ser157Arg
NM_000378.4:c.1105A>C	NP_000369.3:p.Ser369Arg
NM_001198551.1:c.520A>C , LRG_525t2:c.520A>C	NP_001185480.1:p.Ser174Arg
NM_001198552.1:c.469A>C	NP_001185481.1:p.Ser157Arg
NM_024424.3:c.1156A>C	NP_077742.2:p.Ser386Arg
NM_024426.4:c.1156A>C	NP_077744.3:p.Ser386Arg
NM_000378.5:c.1120A>C	NP_000369.4:p.Ser374Arg
NM_024424.4:c.1171A>C	NP_077742.3:p.Ser391Arg
NM_024426.5:c.1171A>C	NP_077744.4:p.Ser391Arg
NM_001367854.1:c.-18A>C	NP_001354783.1:n.-18A>C
NR_160306.1:n.1503A>C
NM_000378.6:c.1120A>C	NP_000369.4:p.Ser374Arg
NM_001198552.2:c.469A>C	NP_001185481.1:p.Ser157Arg
NM_024424.5:c.1171A>C	NP_077742.3:p.Ser391Arg
NM_024426.6:c.1171A>C MANE Select	NP_077744.4:p.Ser391Arg