Canonical Allele Identifier: CA379959172

Gene: WT1

Linked Data

• dbSNP Id: rs2132919788
• COSMIC: COSM21960
• MyVariant Identifiers: chr11:g.32414230G>A (hg19) ; chr11:g.32392684G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392684G>A , CM000673.2:g.32392684G>A	GRCh38
NC_000011.9:g.32414230G>A , CM000673.1:g.32414230G>A	GRCh37
NC_000011.8:g.32370806G>A	NCBI36
NG_009272.1:g.47858C>T , LRG_525:g.47858C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1285C>T	ENSP00000331327.5:p.His429Tyr
ENST00000379077.9:c.*520C>T	ENSP00000368368.5:n.*520C>T
ENST00000379079.8:c.685C>T	ENSP00000368370.2:p.His229Tyr
ENST00000448076.9:c.1336C>T	ENSP00000413452.5:p.His446Tyr
ENST00000452863.10:c.1336C>T MANE Select	ENSP00000415516.5:p.His446Tyr
ENST00000526685.2:n.790C>T
ENST00000639563.3:c.1285C>T	ENSP00000492269.3:p.His429Tyr
ENST00000639907.2:n.479C>T
ENST00000640146.2:c.661C>T	ENSP00000491984.2:p.His221Tyr
ENST00000650745.1:n.545C>T
ENST00000650861.1:n.1917C>T
ENST00000651459.1:c.107C>T
ENST00000651533.1:n.382C>T
ENST00000651668.1:n.273C>T
ENST00000651794.1:n.1179C>T
ENST00000651819.1:n.261C>T
ENST00000652579.1:n.596C>T
ENST00000652724.1:n.526C>T
ENST00000332351.7:c.1321C>T	ENSP00000331327.3:p.His441Tyr
ENST00000379077.7:c.*520C>T	ENSP00000368368.3:n.*520C>T
ENST00000379079.6:c.685C>T	ENSP00000368370.2:p.His229Tyr
ENST00000448076.7:c.1321C>T	ENSP00000413452.3:p.His441Tyr
ENST00000452863.7:c.1270C>T	ENSP00000415516.3:p.His424Tyr
ENST00000527882.5:c.321-620C>T
ENST00000530998.5:c.634C>T	ENSP00000435307.1:p.His212Tyr
NM_000378.4:c.1270C>T	NP_000369.3:p.His424Tyr
NM_001198551.1:c.685C>T , LRG_525t2:c.685C>T	NP_001185480.1:p.His229Tyr
NM_001198552.1:c.634C>T	NP_001185481.1:p.His212Tyr
NM_024424.3:c.1321C>T	NP_077742.2:p.His441Tyr
NM_024426.4:c.1321C>T	NP_077744.3:p.His441Tyr
NM_000378.5:c.1285C>T	NP_000369.4:p.His429Tyr
NM_024424.4:c.1336C>T	NP_077742.3:p.His446Tyr
NM_024426.5:c.1336C>T	NP_077744.4:p.His446Tyr
NM_001367854.1:c.148C>T	NP_001354783.1:p.His50Tyr
NR_160306.1:n.1668C>T
NM_000378.6:c.1285C>T	NP_000369.4:p.His429Tyr
NM_001198552.2:c.634C>T	NP_001185481.1:p.His212Tyr
NM_024424.5:c.1336C>T	NP_077742.3:p.His446Tyr
NM_024426.6:c.1336C>T MANE Select	NP_077744.4:p.His446Tyr