Canonical Allele Identifier: CA10638956
Gene: WT1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32388791C>G , CM000673.2:g.32388791C>G GRCh38
NC_000011.9:g.32410337C>G , CM000673.1:g.32410337C>G GRCh37
NC_000011.8:g.32366913C>G NCBI36
NG_009272.1:g.51751G>C , LRG_525:g.51751G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000332351.9:c.*267G>C ENSP00000331327.5:n.*267G>C
ENST00000379077.9:c.*1020G>C ENSP00000368368.5:n.*1020G>C
ENST00000379079.8:c.*267G>C ENSP00000368370.2:n.*267G>C
ENST00000448076.9:c.*267G>C ENSP00000413452.5:n.*267G>C
ENST00000452863.10:c.*267G>C MANE Select ENSP00000415516.5:n.*267G>C
ENST00000639907.2:n.970G>C
ENST00000640146.2:c.*267G>C ENSP00000491984.2:n.*267G>C
ENST00000650745.1:n.1646G>C
ENST00000650861.1:n.2408G>C
ENST00000651459.1:c.607G>C
ENST00000651533.1:n.873G>C
ENST00000651668.1:n.773G>C
ENST00000651794.1:n.1679G>C
ENST00000651819.1:n.761G>C
ENST00000652579.1:n.1096G>C
ENST00000652724.1:n.1026G>C
ENST00000332351.7:c.*267G>C ENSP00000331327.3:n.*267G>C
ENST00000379077.7:c.*1020G>C ENSP00000368368.3:n.*1020G>C
ENST00000379079.6:c.*267G>C ENSP00000368370.2:n.*267G>C
ENST00000448076.7:c.*267G>C ENSP00000413452.3:n.*267G>C
ENST00000452863.7:c.1761G>C ENSP00000415516.3:n.1761G>C
ENST00000530998.5:c.*267G>C ENSP00000435307.1:n.*267G>C
NM_000378.4:c.*267G>C NP_000369.3:n.*267G>C
NM_001198551.1:c.*267G>C , LRG_525t2:c.*267G>C NP_001185480.1:n.*267G>C
NM_001198552.1:c.*267G>C NP_001185481.1:n.*267G>C
NM_024424.3:c.*267G>C NP_077742.2:n.*267G>C
NM_024426.4:c.*267G>C NP_077744.3:n.*267G>C
NM_000378.5:c.*267G>C NP_000369.4:n.*267G>C
NM_024424.4:c.*267G>C NP_077742.3:n.*267G>C
NM_024426.5:c.*267G>C NP_077744.4:n.*267G>C
NM_001367854.1:c.*267G>C NP_001354783.1:n.*267G>C
NR_160306.1:n.2168G>C
NM_000378.6:c.*267G>C NP_000369.4:n.*267G>C
NM_001198552.2:c.*267G>C NP_001185481.1:n.*267G>C
NM_024424.5:c.*267G>C NP_077742.3:n.*267G>C
NM_024426.6:c.*267G>C MANE Select NP_077744.4:n.*267G>C
Search 100 bp 5'
Search 100 bp 3'