Canonical Allele Identifier: CA1962310461

Gene: WT1

Linked Data

• dbSNP Id: rs1851700333

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32387869G>C , CM000673.2:g.32387869G>C	GRCh38
NC_000011.9:g.32409415G>C , CM000673.1:g.32409415G>C	GRCh37
NC_000011.8:g.32365991G>C	NCBI36
NG_009272.1:g.52673C>G , LRG_525:g.52673C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.*1189C>G	ENSP00000331327.5:n.*1189C>G
ENST00000379077.9:c.*1942C>G	ENSP00000368368.5:n.*1942C>G
ENST00000379079.8:c.*1189C>G	ENSP00000368370.2:n.*1189C>G
ENST00000452863.10:c.*1189C>G MANE Select	ENSP00000415516.5:n.*1189C>G
ENST00000332351.7:c.*1189C>G	ENSP00000331327.3:n.*1189C>G
ENST00000379077.7:c.*1942C>G	ENSP00000368368.3:n.*1942C>G
ENST00000379079.6:c.*1189C>G	ENSP00000368370.2:n.*1189C>G
ENST00000452863.7:c.2683C>G	ENSP00000415516.3:n.2683C>G
ENST00000530998.5:c.*1189C>G	ENSP00000435307.1:n.*1189C>G
NM_000378.4:c.*1189C>G	NP_000369.3:n.*1189C>G
NM_001198551.1:c.*1189C>G , LRG_525t2:c.*1189C>G	NP_001185480.1:n.*1189C>G
NM_001198552.1:c.*1189C>G	NP_001185481.1:n.*1189C>G
NM_024424.3:c.*1189C>G	NP_077742.2:n.*1189C>G
NM_024426.4:c.*1189C>G	NP_077744.3:n.*1189C>G
NM_000378.5:c.*1189C>G	NP_000369.4:n.*1189C>G
NM_024424.4:c.*1189C>G	NP_077742.3:n.*1189C>G
NM_024426.5:c.*1189C>G	NP_077744.4:n.*1189C>G
NM_001367854.1:c.*1189C>G	NP_001354783.1:n.*1189C>G
NR_160306.1:n.3090C>G
NM_000378.6:c.*1189C>G	NP_000369.4:n.*1189C>G
NM_001198552.2:c.*1189C>G	NP_001185481.1:n.*1189C>G
NM_024424.5:c.*1189C>G	NP_077742.3:n.*1189C>G
NM_024426.6:c.*1189C>G MANE Select	NP_077744.4:n.*1189C>G