Canonical Allele Identifier: CA379958844

Gene: WT1

Linked Data

• dbSNP Id: rs2132914435
• MyVariant Identifiers: chr11:g.32413563A>G (hg19) ; chr11:g.32392017A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392017A>G , CM000673.2:g.32392017A>G	GRCh38
NC_000011.9:g.32413563A>G , CM000673.1:g.32413563A>G	GRCh37
NC_000011.8:g.32370139A>G	NCBI36
NG_009272.1:g.48525T>C , LRG_525:g.48525T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1351T>C	ENSP00000331327.5:p.Ser451Pro
ENST00000379077.9:c.*586T>C	ENSP00000368368.5:n.*586T>C
ENST00000379079.8:c.751T>C	ENSP00000368370.2:p.Ser251Pro
ENST00000448076.9:c.1402T>C	ENSP00000413452.5:p.Ser468Pro
ENST00000452863.10:c.1402T>C MANE Select	ENSP00000415516.5:p.Ser468Pro
ENST00000526685.2:n.856T>C
ENST00000639563.3:c.1351T>C	ENSP00000492269.3:p.Ser451Pro
ENST00000639907.2:n.545T>C
ENST00000640146.2:c.727T>C	ENSP00000491984.2:p.Ser243Pro
ENST00000650745.1:n.1212T>C
ENST00000650861.1:n.1983T>C
ENST00000650986.1:n.65T>C
ENST00000651459.1:c.173T>C
ENST00000651533.1:n.448T>C
ENST00000651668.1:n.339T>C
ENST00000651794.1:n.1245T>C
ENST00000651819.1:n.327T>C
ENST00000652579.1:n.662T>C
ENST00000652724.1:n.592T>C
ENST00000332351.7:c.1387T>C	ENSP00000331327.3:p.Ser463Pro
ENST00000379077.7:c.*586T>C	ENSP00000368368.3:n.*586T>C
ENST00000379079.6:c.751T>C	ENSP00000368370.2:p.Ser251Pro
ENST00000448076.7:c.1387T>C	ENSP00000413452.3:p.Ser463Pro
ENST00000452863.7:c.1336T>C	ENSP00000415516.3:p.Ser446Pro
ENST00000527882.5:c.368T>C
ENST00000530998.5:c.700T>C	ENSP00000435307.1:p.Ser234Pro
NM_000378.4:c.1336T>C	NP_000369.3:p.Ser446Pro
NM_001198551.1:c.751T>C , LRG_525t2:c.751T>C	NP_001185480.1:p.Ser251Pro
NM_001198552.1:c.700T>C	NP_001185481.1:p.Ser234Pro
NM_024424.3:c.1387T>C	NP_077742.2:p.Ser463Pro
NM_024426.4:c.1387T>C	NP_077744.3:p.Ser463Pro
NM_000378.5:c.1351T>C	NP_000369.4:p.Ser451Pro
NM_024424.4:c.1402T>C	NP_077742.3:p.Ser468Pro
NM_024426.5:c.1402T>C	NP_077744.4:p.Ser468Pro
NM_001367854.1:c.214T>C	NP_001354783.1:p.Ser72Pro
NR_160306.1:n.1734T>C
NM_000378.6:c.1351T>C	NP_000369.4:p.Ser451Pro
NM_001198552.2:c.700T>C	NP_001185481.1:p.Ser234Pro
NM_024424.5:c.1402T>C	NP_077742.3:p.Ser468Pro
NM_024426.6:c.1402T>C MANE Select	NP_077744.4:p.Ser468Pro