Canonical Allele Identifier: CA10634638
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 304378
dbSNP Id: rs58549495

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32388032_32388037dup , CM000673.2:g.32388032_32388037dup GRCh38
NC_000011.9:g.32409578_32409583dup , CM000673.1:g.32409578_32409583dup GRCh37
NC_000011.8:g.32366154_32366159dup NCBI36
NG_009272.1:g.52533_52538dup , LRG_525:g.52533_52538dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000332351.9:c.*1049_*1054dup ENSP00000331327.5:n.*1049_*1054dup
ENST00000379077.9:c.*1802_*1807dup ENSP00000368368.5:n.*1802_*1807dup
ENST00000379079.8:c.*1049_*1054dup ENSP00000368370.2:n.*1049_*1054dup
ENST00000452863.10:c.*1049_*1054dup MANE Select ENSP00000415516.5:n.*1049_*1054dup
ENST00000651819.1:n.1543_1548dup
ENST00000332351.7:c.*1049_*1054dup ENSP00000331327.3:n.*1049_*1054dup
ENST00000379077.7:c.*1802_*1807dup ENSP00000368368.3:n.*1802_*1807dup
ENST00000379079.6:c.*1049_*1054dup ENSP00000368370.2:n.*1049_*1054dup
ENST00000452863.7:c.2543_2548dup ENSP00000415516.3:n.2543_2548dup
ENST00000530998.5:c.*1049_*1054dup ENSP00000435307.1:n.*1049_*1054dup
NM_000378.4:c.*1049_*1054dup NP_000369.3:n.*1049_*1054dup
NM_001198551.1:c.*1049_*1054dup , LRG_525t2:c.*1049_*1054dup NP_001185480.1:n.*1049_*1054dup
NM_001198552.1:c.*1049_*1054dup NP_001185481.1:n.*1049_*1054dup
NM_024424.3:c.*1049_*1054dup NP_077742.2:n.*1049_*1054dup
NM_024426.4:c.*1049_*1054dup NP_077744.3:n.*1049_*1054dup
NM_000378.5:c.*1049_*1054dup NP_000369.4:n.*1049_*1054dup
NM_024424.4:c.*1049_*1054dup NP_077742.3:n.*1049_*1054dup
NM_024426.5:c.*1049_*1054dup NP_077744.4:n.*1049_*1054dup
NM_001367854.1:c.*1049_*1054dup NP_001354783.1:n.*1049_*1054dup
NR_160306.1:n.2950_2955dup
NM_000378.6:c.*1049_*1054dup NP_000369.4:n.*1049_*1054dup
NM_001198552.2:c.*1049_*1054dup NP_001185481.1:n.*1049_*1054dup
NM_024424.5:c.*1049_*1054dup NP_077742.3:n.*1049_*1054dup
NM_024426.6:c.*1049_*1054dup MANE Select NP_077744.4:n.*1049_*1054dup