Canonical Allele Identifier: CA473565372

Gene: WT1

Linked Data

• MyVariant Identifiers: chr11:g.32413567G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392021G>T , CM000673.2:g.32392021G>T	GRCh38
NC_000011.9:g.32413567G>T , CM000673.1:g.32413567G>T	GRCh37
NC_000011.8:g.32370143G>T	NCBI36
NG_009272.1:g.48521C>A , LRG_525:g.48521C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1347C>A	ENSP00000331327.5:p.Ser449=
ENST00000379077.9:c.*582C>A	ENSP00000368368.5:n.*582C>A
ENST00000379079.8:c.747C>A	ENSP00000368370.2:p.Ser249=
ENST00000448076.9:c.1398C>A	ENSP00000413452.5:p.Ser466=
ENST00000452863.10:c.1398C>A MANE Select	ENSP00000415516.5:p.Ser466=
ENST00000526685.2:n.852C>A
ENST00000639563.3:c.1347C>A	ENSP00000492269.3:p.Ser449=
ENST00000639907.2:n.541C>A
ENST00000640146.2:c.723C>A	ENSP00000491984.2:p.Ser241=
ENST00000650745.1:n.1208C>A
ENST00000650861.1:n.1979C>A
ENST00000650986.1:n.61C>A
ENST00000651459.1:c.169C>A
ENST00000651533.1:n.444C>A
ENST00000651668.1:n.335C>A
ENST00000651794.1:n.1241C>A
ENST00000651819.1:n.323C>A
ENST00000652579.1:n.658C>A
ENST00000652724.1:n.588C>A
ENST00000332351.7:c.1383C>A	ENSP00000331327.3:p.Ser461=
ENST00000379077.7:c.*582C>A	ENSP00000368368.3:n.*582C>A
ENST00000379079.6:c.747C>A	ENSP00000368370.2:p.Ser249=
ENST00000448076.7:c.1383C>A	ENSP00000413452.3:p.Ser461=
ENST00000452863.7:c.1332C>A	ENSP00000415516.3:p.Ser444=
ENST00000527882.5:c.364C>A
ENST00000530998.5:c.696C>A	ENSP00000435307.1:p.Ser232=
NM_000378.4:c.1332C>A	NP_000369.3:p.Ser444=
NM_001198551.1:c.747C>A , LRG_525t2:c.747C>A	NP_001185480.1:p.Ser249=
NM_001198552.1:c.696C>A	NP_001185481.1:p.Ser232=
NM_024424.3:c.1383C>A	NP_077742.2:p.Ser461=
NM_024426.4:c.1383C>A	NP_077744.3:p.Ser461=
NM_000378.5:c.1347C>A	NP_000369.4:p.Ser449=
NM_024424.4:c.1398C>A	NP_077742.3:p.Ser466=
NM_024426.5:c.1398C>A	NP_077744.4:p.Ser466=
NM_001367854.1:c.210C>A	NP_001354783.1:p.Ser70=
NR_160306.1:n.1730C>A
NM_000378.6:c.1347C>A	NP_000369.4:p.Ser449=
NM_001198552.2:c.696C>A	NP_001185481.1:p.Ser232=
NM_024424.5:c.1398C>A	NP_077742.3:p.Ser466=
NM_024426.6:c.1398C>A MANE Select	NP_077744.4:p.Ser466=