Canonical Allele Identifier: CA379959879

Gene: WT1

Linked Data

• MyVariant Identifiers: chr11:g.32417853T>G (hg19) ; chr11:g.32396307T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32396307T>G , CM000673.2:g.32396307T>G	GRCh38
NC_000011.9:g.32417853T>G , CM000673.1:g.32417853T>G	GRCh37
NC_000011.8:g.32374429T>G	NCBI36
NG_009272.1:g.44235A>C , LRG_525:g.44235A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1163A>C	ENSP00000331327.5:p.Lys388Thr
ENST00000379077.9:c.*398A>C	ENSP00000368368.5:n.*398A>C
ENST00000379079.8:c.563A>C	ENSP00000368370.2:p.Lys188Thr
ENST00000448076.9:c.1214A>C	ENSP00000413452.5:p.Lys405Thr
ENST00000452863.10:c.1214A>C MANE Select	ENSP00000415516.5:p.Lys405Thr
ENST00000526685.2:n.668A>C
ENST00000639563.3:c.1163A>C	ENSP00000492269.3:p.Lys388Thr
ENST00000639907.2:n.357A>C
ENST00000640146.2:c.539A>C	ENSP00000491984.2:p.Lys180Thr
ENST00000650861.1:n.1795A>C
ENST00000651459.1:c.36-3552A>C
ENST00000651668.1:n.151A>C
ENST00000651794.1:n.957A>C
ENST00000651819.1:n.139A>C
ENST00000652579.1:n.374A>C
ENST00000652724.1:n.404A>C
ENST00000332351.7:c.1199A>C	ENSP00000331327.3:p.Lys400Thr
ENST00000379077.7:c.*398A>C	ENSP00000368368.3:n.*398A>C
ENST00000379079.6:c.563A>C	ENSP00000368370.2:p.Lys188Thr
ENST00000448076.7:c.1199A>C	ENSP00000413452.3:p.Lys400Thr
ENST00000452863.7:c.1148A>C	ENSP00000415516.3:p.Lys383Thr
ENST00000526685.1:c.26A>C	ENSP00000436292.1:p.Lys9Thr
ENST00000527882.5:c.270A>C
ENST00000530998.5:c.512A>C	ENSP00000435307.1:p.Lys171Thr
NM_000378.4:c.1148A>C	NP_000369.3:p.Lys383Thr
NM_001198551.1:c.563A>C , LRG_525t2:c.563A>C	NP_001185480.1:p.Lys188Thr
NM_001198552.1:c.512A>C	NP_001185481.1:p.Lys171Thr
NM_024424.3:c.1199A>C	NP_077742.2:p.Lys400Thr
NM_024426.4:c.1199A>C	NP_077744.3:p.Lys400Thr
NM_000378.5:c.1163A>C	NP_000369.4:p.Lys388Thr
NM_024424.4:c.1214A>C	NP_077742.3:p.Lys405Thr
NM_024426.5:c.1214A>C	NP_077744.4:p.Lys405Thr
NM_001367854.1:c.26A>C	NP_001354783.1:p.Lys9Thr
NR_160306.1:n.1546A>C
NM_000378.6:c.1163A>C	NP_000369.4:p.Lys388Thr
NM_001198552.2:c.512A>C	NP_001185481.1:p.Lys171Thr
NM_024424.5:c.1214A>C	NP_077742.3:p.Lys405Thr
NM_024426.6:c.1214A>C MANE Select	NP_077744.4:p.Lys405Thr