Canonical Allele Identifier: CA379958661

Gene: WT1

Linked Data

• COSMIC: COSM369494
• MyVariant Identifiers: chr11:g.32413521T>G (hg19) ; chr11:g.32391975T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32391975T>G , CM000673.2:g.32391975T>G	GRCh38
NC_000011.9:g.32413521T>G , CM000673.1:g.32413521T>G	GRCh37
NC_000011.8:g.32370097T>G	NCBI36
NG_009272.1:g.48567A>C , LRG_525:g.48567A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1387+6A>C	ENSP00000331327.5:n.1387+6A>C
ENST00000379077.9:c.*628A>C	ENSP00000368368.5:n.*628A>C
ENST00000379079.8:c.787+6A>C	ENSP00000368370.2:n.787+6A>C
ENST00000448076.9:c.1438+6A>C	ENSP00000413452.5:n.1438+6A>C
ENST00000452863.10:c.1444A>C MANE Select	ENSP00000415516.5:p.Thr482Pro
ENST00000526685.2:n.892+6A>C
ENST00000639563.3:c.1393A>C	ENSP00000492269.3:p.Thr465Pro
ENST00000639907.2:n.581+6A>C
ENST00000640146.2:c.769A>C	ENSP00000491984.2:p.Thr257Pro
ENST00000650745.1:n.1254A>C
ENST00000650861.1:n.2019+6A>C
ENST00000650986.1:n.107A>C
ENST00000651459.1:c.215A>C
ENST00000651533.1:n.484+6A>C
ENST00000651668.1:n.381A>C
ENST00000651794.1:n.1287A>C
ENST00000651819.1:n.369A>C
ENST00000652579.1:n.704A>C
ENST00000652724.1:n.634A>C
ENST00000332351.7:c.1429A>C	ENSP00000331327.3:p.Thr477Pro
ENST00000379077.7:c.*628A>C	ENSP00000368368.3:n.*628A>C
ENST00000379079.6:c.787+6A>C	ENSP00000368370.2:n.787+6A>C
ENST00000448076.7:c.1423+6A>C	ENSP00000413452.3:n.1423+6A>C
ENST00000452863.7:c.1372+6A>C	ENSP00000415516.3:n.1372+6A>C
ENST00000527882.5:c.410A>C
ENST00000530998.5:c.742A>C	ENSP00000435307.1:p.Thr248Pro
NM_000378.4:c.1372+6A>C	NP_000369.3:n.1372+6A>C
NM_001198551.1:c.787+6A>C , LRG_525t2:c.787+6A>C	NP_001185480.1:n.787+6A>C
NM_001198552.1:c.742A>C	NP_001185481.1:p.Thr248Pro
NM_024424.3:c.1423+6A>C	NP_077742.2:n.1423+6A>C
NM_024426.4:c.1429A>C	NP_077744.3:p.Thr477Pro
NM_000378.5:c.1387+6A>C	NP_000369.4:n.1387+6A>C
NM_024424.4:c.1438+6A>C	NP_077742.3:n.1438+6A>C
NM_024426.5:c.1444A>C	NP_077744.4:p.Thr482Pro
NM_001367854.1:c.256A>C	NP_001354783.1:p.Thr86Pro
NR_160306.1:n.1776A>C
NM_000378.6:c.1387+6A>C	NP_000369.4:n.1387+6A>C
NM_001198552.2:c.742A>C	NP_001185481.1:p.Thr248Pro
NM_024424.5:c.1438+6A>C	NP_077742.3:n.1438+6A>C
NM_024426.6:c.1444A>C MANE Select	NP_077744.4:p.Thr482Pro