Canonical Allele Identifier: CA379959351

Gene: WT1

Linked Data

• dbSNP Id: rs2132920974
• COSMIC: COSM6068561 ; COSM6068562 ; COSM6068563
• MyVariant Identifiers: chr11:g.32414272C>A (hg19) ; chr11:g.32392726C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392726C>A , CM000673.2:g.32392726C>A	GRCh38
NC_000011.9:g.32414272C>A , CM000673.1:g.32414272C>A	GRCh37
NC_000011.8:g.32370848C>A	NCBI36
NG_009272.1:g.47816G>T , LRG_525:g.47816G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1243G>T	ENSP00000331327.5:p.Asp415Tyr
ENST00000379077.9:c.*478G>T	ENSP00000368368.5:n.*478G>T
ENST00000379079.8:c.643G>T	ENSP00000368370.2:p.Asp215Tyr
ENST00000448076.9:c.1294G>T	ENSP00000413452.5:p.Asp432Tyr
ENST00000452863.10:c.1294G>T MANE Select	ENSP00000415516.5:p.Asp432Tyr
ENST00000526685.2:n.748G>T
ENST00000639563.3:c.1243G>T	ENSP00000492269.3:p.Asp415Tyr
ENST00000639907.2:n.437G>T
ENST00000640146.2:c.619G>T	ENSP00000491984.2:p.Asp207Tyr
ENST00000650745.1:n.503G>T
ENST00000650861.1:n.1875G>T
ENST00000651459.1:c.65G>T
ENST00000651533.1:n.340G>T
ENST00000651668.1:n.231G>T
ENST00000651794.1:n.1137G>T
ENST00000651819.1:n.219G>T
ENST00000652579.1:n.554G>T
ENST00000652724.1:n.484G>T
ENST00000332351.7:c.1279G>T	ENSP00000331327.3:p.Asp427Tyr
ENST00000379077.7:c.*478G>T	ENSP00000368368.3:n.*478G>T
ENST00000379079.6:c.643G>T	ENSP00000368370.2:p.Asp215Tyr
ENST00000448076.7:c.1279G>T	ENSP00000413452.3:p.Asp427Tyr
ENST00000452863.7:c.1228G>T	ENSP00000415516.3:p.Asp410Tyr
ENST00000527882.5:c.321-662G>T
ENST00000530998.5:c.592G>T	ENSP00000435307.1:p.Asp198Tyr
NM_000378.4:c.1228G>T	NP_000369.3:p.Asp410Tyr
NM_001198551.1:c.643G>T , LRG_525t2:c.643G>T	NP_001185480.1:p.Asp215Tyr
NM_001198552.1:c.592G>T	NP_001185481.1:p.Asp198Tyr
NM_024424.3:c.1279G>T	NP_077742.2:p.Asp427Tyr
NM_024426.4:c.1279G>T	NP_077744.3:p.Asp427Tyr
NM_000378.5:c.1243G>T	NP_000369.4:p.Asp415Tyr
NM_024424.4:c.1294G>T	NP_077742.3:p.Asp432Tyr
NM_024426.5:c.1294G>T	NP_077744.4:p.Asp432Tyr
NM_001367854.1:c.106G>T	NP_001354783.1:p.Asp36Tyr
NR_160306.1:n.1626G>T
NM_000378.6:c.1243G>T	NP_000369.4:p.Asp415Tyr
NM_001198552.2:c.592G>T	NP_001185481.1:p.Asp198Tyr
NM_024424.5:c.1294G>T	NP_077742.3:p.Asp432Tyr
NM_024426.6:c.1294G>T MANE Select	NP_077744.4:p.Asp432Tyr