Canonical Allele Identifier: CA473565262

Gene: WT1

Linked Data

• MyVariant Identifiers: chr11:g.32413528T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32391982T>A , CM000673.2:g.32391982T>A	GRCh38
NC_000011.9:g.32413528T>A , CM000673.1:g.32413528T>A	GRCh37
NC_000011.8:g.32370104T>A	NCBI36
NG_009272.1:g.48560A>T , LRG_525:g.48560A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1386A>T	ENSP00000331327.5:p.Thr462=
ENST00000379077.9:c.*621A>T	ENSP00000368368.5:n.*621A>T
ENST00000379079.8:c.786A>T	ENSP00000368370.2:p.Thr262=
ENST00000448076.9:c.1437A>T	ENSP00000413452.5:p.Thr479=
ENST00000452863.10:c.1437A>T MANE Select	ENSP00000415516.5:p.Thr479=
ENST00000526685.2:n.891A>T
ENST00000639563.3:c.1386A>T	ENSP00000492269.3:p.Thr462=
ENST00000639907.2:n.580A>T
ENST00000640146.2:c.762A>T	ENSP00000491984.2:p.Thr254=
ENST00000650745.1:n.1247A>T
ENST00000650861.1:n.2018A>T
ENST00000650986.1:n.100A>T
ENST00000651459.1:c.208A>T
ENST00000651533.1:n.483A>T
ENST00000651668.1:n.374A>T
ENST00000651794.1:n.1280A>T
ENST00000651819.1:n.362A>T
ENST00000652579.1:n.697A>T
ENST00000652724.1:n.627A>T
ENST00000332351.7:c.1422A>T	ENSP00000331327.3:p.Thr474=
ENST00000379077.7:c.*621A>T	ENSP00000368368.3:n.*621A>T
ENST00000379079.6:c.786A>T	ENSP00000368370.2:p.Thr262=
ENST00000448076.7:c.1422A>T	ENSP00000413452.3:p.Thr474=
ENST00000452863.7:c.1371A>T	ENSP00000415516.3:p.Thr457=
ENST00000527882.5:c.403A>T
ENST00000530998.5:c.735A>T	ENSP00000435307.1:p.Thr245=
NM_000378.4:c.1371A>T	NP_000369.3:p.Thr457=
NM_001198551.1:c.786A>T , LRG_525t2:c.786A>T	NP_001185480.1:p.Thr262=
NM_001198552.1:c.735A>T	NP_001185481.1:p.Thr245=
NM_024424.3:c.1422A>T	NP_077742.2:p.Thr474=
NM_024426.4:c.1422A>T	NP_077744.3:p.Thr474=
NM_000378.5:c.1386A>T	NP_000369.4:p.Thr462=
NM_024424.4:c.1437A>T	NP_077742.3:p.Thr479=
NM_024426.5:c.1437A>T	NP_077744.4:p.Thr479=
NM_001367854.1:c.249A>T	NP_001354783.1:p.Thr83=
NR_160306.1:n.1769A>T
NM_000378.6:c.1386A>T	NP_000369.4:p.Thr462=
NM_001198552.2:c.735A>T	NP_001185481.1:p.Thr245=
NM_024424.5:c.1437A>T	NP_077742.3:p.Thr479=
NM_024426.6:c.1437A>T MANE Select	NP_077744.4:p.Thr479=