Canonical Allele Identifier: CA379959171

Gene: WT1

Linked Data

• MyVariant Identifiers: chr11:g.32414229T>G (hg19) ; chr11:g.32392683T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392683T>G , CM000673.2:g.32392683T>G	GRCh38
NC_000011.9:g.32414229T>G , CM000673.1:g.32414229T>G	GRCh37
NC_000011.8:g.32370805T>G	NCBI36
NG_009272.1:g.47859A>C , LRG_525:g.47859A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1286A>C	ENSP00000331327.5:p.His429Pro
ENST00000379077.9:c.*521A>C	ENSP00000368368.5:n.*521A>C
ENST00000379079.8:c.686A>C	ENSP00000368370.2:p.His229Pro
ENST00000448076.9:c.1337A>C	ENSP00000413452.5:p.His446Pro
ENST00000452863.10:c.1337A>C MANE Select	ENSP00000415516.5:p.His446Pro
ENST00000526685.2:n.791A>C
ENST00000639563.3:c.1286A>C	ENSP00000492269.3:p.His429Pro
ENST00000639907.2:n.480A>C
ENST00000640146.2:c.662A>C	ENSP00000491984.2:p.His221Pro
ENST00000650745.1:n.546A>C
ENST00000650861.1:n.1918A>C
ENST00000651459.1:c.108A>C
ENST00000651533.1:n.383A>C
ENST00000651668.1:n.274A>C
ENST00000651794.1:n.1180A>C
ENST00000651819.1:n.262A>C
ENST00000652579.1:n.597A>C
ENST00000652724.1:n.527A>C
ENST00000332351.7:c.1322A>C	ENSP00000331327.3:p.His441Pro
ENST00000379077.7:c.*521A>C	ENSP00000368368.3:n.*521A>C
ENST00000379079.6:c.686A>C	ENSP00000368370.2:p.His229Pro
ENST00000448076.7:c.1322A>C	ENSP00000413452.3:p.His441Pro
ENST00000452863.7:c.1271A>C	ENSP00000415516.3:p.His424Pro
ENST00000527882.5:c.321-619A>C
ENST00000530998.5:c.635A>C	ENSP00000435307.1:p.His212Pro
NM_000378.4:c.1271A>C	NP_000369.3:p.His424Pro
NM_001198551.1:c.686A>C , LRG_525t2:c.686A>C	NP_001185480.1:p.His229Pro
NM_001198552.1:c.635A>C	NP_001185481.1:p.His212Pro
NM_024424.3:c.1322A>C	NP_077742.2:p.His441Pro
NM_024426.4:c.1322A>C	NP_077744.3:p.His441Pro
NM_000378.5:c.1286A>C	NP_000369.4:p.His429Pro
NM_024424.4:c.1337A>C	NP_077742.3:p.His446Pro
NM_024426.5:c.1337A>C	NP_077744.4:p.His446Pro
NM_001367854.1:c.149A>C	NP_001354783.1:p.His50Pro
NR_160306.1:n.1669A>C
NM_000378.6:c.1286A>C	NP_000369.4:p.His429Pro
NM_001198552.2:c.635A>C	NP_001185481.1:p.His212Pro
NM_024424.5:c.1337A>C	NP_077742.3:p.His446Pro
NM_024426.6:c.1337A>C MANE Select	NP_077744.4:p.His446Pro