Canonical Allele Identifier: CA473565247

Gene: WT1

Linked Data

• MyVariant Identifiers: chr11:g.32413519T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32391973T>G , CM000673.2:g.32391973T>G	GRCh38
NC_000011.9:g.32413519T>G , CM000673.1:g.32413519T>G	GRCh37
NC_000011.8:g.32370095T>G	NCBI36
NG_009272.1:g.48569A>C , LRG_525:g.48569A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1387+8A>C	ENSP00000331327.5:n.1387+8A>C
ENST00000379077.9:c.*630A>C	ENSP00000368368.5:n.*630A>C
ENST00000379079.8:c.787+8A>C	ENSP00000368370.2:n.787+8A>C
ENST00000448076.9:c.1438+8A>C	ENSP00000413452.5:n.1438+8A>C
ENST00000452863.10:c.1446A>C MANE Select	ENSP00000415516.5:p.Thr482=
ENST00000526685.2:n.892+8A>C
ENST00000639563.3:c.1395A>C	ENSP00000492269.3:p.Thr465=
ENST00000639907.2:n.581+8A>C
ENST00000640146.2:c.771A>C	ENSP00000491984.2:p.Thr257=
ENST00000650745.1:n.1256A>C
ENST00000650861.1:n.2019+8A>C
ENST00000650986.1:n.109A>C
ENST00000651459.1:c.217A>C
ENST00000651533.1:n.484+8A>C
ENST00000651668.1:n.383A>C
ENST00000651794.1:n.1289A>C
ENST00000651819.1:n.371A>C
ENST00000652579.1:n.706A>C
ENST00000652724.1:n.636A>C
ENST00000332351.7:c.1431A>C	ENSP00000331327.3:p.Thr477=
ENST00000379077.7:c.*630A>C	ENSP00000368368.3:n.*630A>C
ENST00000379079.6:c.787+8A>C	ENSP00000368370.2:n.787+8A>C
ENST00000448076.7:c.1423+8A>C	ENSP00000413452.3:n.1423+8A>C
ENST00000452863.7:c.1372+8A>C	ENSP00000415516.3:n.1372+8A>C
ENST00000527882.5:c.412A>C
ENST00000530998.5:c.744A>C	ENSP00000435307.1:p.Thr248=
NM_000378.4:c.1372+8A>C	NP_000369.3:n.1372+8A>C
NM_001198551.1:c.787+8A>C , LRG_525t2:c.787+8A>C	NP_001185480.1:n.787+8A>C
NM_001198552.1:c.744A>C	NP_001185481.1:p.Thr248=
NM_024424.3:c.1423+8A>C	NP_077742.2:n.1423+8A>C
NM_024426.4:c.1431A>C	NP_077744.3:p.Thr477=
NM_000378.5:c.1387+8A>C	NP_000369.4:n.1387+8A>C
NM_024424.4:c.1438+8A>C	NP_077742.3:n.1438+8A>C
NM_024426.5:c.1446A>C	NP_077744.4:p.Thr482=
NM_001367854.1:c.258A>C	NP_001354783.1:p.Thr86=
NR_160306.1:n.1778A>C
NM_000378.6:c.1387+8A>C	NP_000369.4:n.1387+8A>C
NM_001198552.2:c.744A>C	NP_001185481.1:p.Thr248=
NM_024424.5:c.1438+8A>C	NP_077742.3:n.1438+8A>C
NM_024426.6:c.1446A>C MANE Select	NP_077744.4:p.Thr482=