Canonical Allele Identifier: CA473565792

Gene: WT1

Linked Data

• dbSNP Id: rs2132920008
• MyVariant Identifiers: chr11:g.32414237G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392691G>A , CM000673.2:g.32392691G>A	GRCh38
NC_000011.9:g.32414237G>A , CM000673.1:g.32414237G>A	GRCh37
NC_000011.8:g.32370813G>A	NCBI36
NG_009272.1:g.47851C>T , LRG_525:g.47851C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1278C>T	ENSP00000331327.5:p.Leu426=
ENST00000379077.9:c.*513C>T	ENSP00000368368.5:n.*513C>T
ENST00000379079.8:c.678C>T	ENSP00000368370.2:p.Leu226=
ENST00000448076.9:c.1329C>T	ENSP00000413452.5:p.Leu443=
ENST00000452863.10:c.1329C>T MANE Select	ENSP00000415516.5:p.Leu443=
ENST00000526685.2:n.783C>T
ENST00000639563.3:c.1278C>T	ENSP00000492269.3:p.Leu426=
ENST00000639907.2:n.472C>T
ENST00000640146.2:c.654C>T	ENSP00000491984.2:p.Leu218=
ENST00000650745.1:n.538C>T
ENST00000650861.1:n.1910C>T
ENST00000651459.1:c.100C>T
ENST00000651533.1:n.375C>T
ENST00000651668.1:n.266C>T
ENST00000651794.1:n.1172C>T
ENST00000651819.1:n.254C>T
ENST00000652579.1:n.589C>T
ENST00000652724.1:n.519C>T
ENST00000332351.7:c.1314C>T	ENSP00000331327.3:p.Leu438=
ENST00000379077.7:c.*513C>T	ENSP00000368368.3:n.*513C>T
ENST00000379079.6:c.678C>T	ENSP00000368370.2:p.Leu226=
ENST00000448076.7:c.1314C>T	ENSP00000413452.3:p.Leu438=
ENST00000452863.7:c.1263C>T	ENSP00000415516.3:p.Leu421=
ENST00000527882.5:c.321-627C>T
ENST00000530998.5:c.627C>T	ENSP00000435307.1:p.Leu209=
NM_000378.4:c.1263C>T	NP_000369.3:p.Leu421=
NM_001198551.1:c.678C>T , LRG_525t2:c.678C>T	NP_001185480.1:p.Leu226=
NM_001198552.1:c.627C>T	NP_001185481.1:p.Leu209=
NM_024424.3:c.1314C>T	NP_077742.2:p.Leu438=
NM_024426.4:c.1314C>T	NP_077744.3:p.Leu438=
NM_000378.5:c.1278C>T	NP_000369.4:p.Leu426=
NM_024424.4:c.1329C>T	NP_077742.3:p.Leu443=
NM_024426.5:c.1329C>T	NP_077744.4:p.Leu443=
NM_001367854.1:c.141C>T	NP_001354783.1:p.Leu47=
NR_160306.1:n.1661C>T
NM_000378.6:c.1278C>T	NP_000369.4:p.Leu426=
NM_001198552.2:c.627C>T	NP_001185481.1:p.Leu209=
NM_024424.5:c.1329C>T	NP_077742.3:p.Leu443=
NM_024426.6:c.1329C>T MANE Select	NP_077744.4:p.Leu443=