Canonical Allele Identifier: CA379959180

Gene: WT1

Linked Data

• dbSNP Id: rs2132919864
• MyVariant Identifiers: chr11:g.32414233T>A (hg19) ; chr11:g.32392687T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392687T>A , CM000673.2:g.32392687T>A	GRCh38
NC_000011.9:g.32414233T>A , CM000673.1:g.32414233T>A	GRCh37
NC_000011.8:g.32370809T>A	NCBI36
NG_009272.1:g.47855A>T , LRG_525:g.47855A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1282A>T	ENSP00000331327.5:p.Arg428Ter
ENST00000379077.9:c.*517A>T	ENSP00000368368.5:n.*517A>T
ENST00000379079.8:c.682A>T	ENSP00000368370.2:p.Arg228Ter
ENST00000448076.9:c.1333A>T	ENSP00000413452.5:p.Arg445Ter
ENST00000452863.10:c.1333A>T MANE Select	ENSP00000415516.5:p.Arg445Ter
ENST00000526685.2:n.787A>T
ENST00000639563.3:c.1282A>T	ENSP00000492269.3:p.Arg428Ter
ENST00000639907.2:n.476A>T
ENST00000640146.2:c.658A>T	ENSP00000491984.2:p.Arg220Ter
ENST00000650745.1:n.542A>T
ENST00000650861.1:n.1914A>T
ENST00000651459.1:c.104A>T
ENST00000651533.1:n.379A>T
ENST00000651668.1:n.270A>T
ENST00000651794.1:n.1176A>T
ENST00000651819.1:n.258A>T
ENST00000652579.1:n.593A>T
ENST00000652724.1:n.523A>T
ENST00000332351.7:c.1318A>T	ENSP00000331327.3:p.Arg440Ter
ENST00000379077.7:c.*517A>T	ENSP00000368368.3:n.*517A>T
ENST00000379079.6:c.682A>T	ENSP00000368370.2:p.Arg228Ter
ENST00000448076.7:c.1318A>T	ENSP00000413452.3:p.Arg440Ter
ENST00000452863.7:c.1267A>T	ENSP00000415516.3:p.Arg423Ter
ENST00000527882.5:c.321-623A>T
ENST00000530998.5:c.631A>T	ENSP00000435307.1:p.Arg211Ter
NM_000378.4:c.1267A>T	NP_000369.3:p.Arg423Ter
NM_001198551.1:c.682A>T , LRG_525t2:c.682A>T	NP_001185480.1:p.Arg228Ter
NM_001198552.1:c.631A>T	NP_001185481.1:p.Arg211Ter
NM_024424.3:c.1318A>T	NP_077742.2:p.Arg440Ter
NM_024426.4:c.1318A>T	NP_077744.3:p.Arg440Ter
NM_000378.5:c.1282A>T	NP_000369.4:p.Arg428Ter
NM_024424.4:c.1333A>T	NP_077742.3:p.Arg445Ter
NM_024426.5:c.1333A>T	NP_077744.4:p.Arg445Ter
NM_001367854.1:c.145A>T	NP_001354783.1:p.Arg49Ter
NR_160306.1:n.1665A>T
NM_000378.6:c.1282A>T	NP_000369.4:p.Arg428Ter
NM_001198552.2:c.631A>T	NP_001185481.1:p.Arg211Ter
NM_024424.5:c.1333A>T	NP_077742.3:p.Arg445Ter
NM_024426.6:c.1333A>T MANE Select	NP_077744.4:p.Arg445Ter