Canonical Allele Identifier: CA2612972947

Gene: WT1

Linked Data

• gnomAD v4: 11-32392609-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392609A>C , CM000673.2:g.32392609A>C	GRCh38
NC_000011.9:g.32414155A>C , CM000673.1:g.32414155A>C	GRCh37
NC_000011.8:g.32370731A>C	NCBI36
NG_009272.1:g.47933T>G , LRG_525:g.47933T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1303+57T>G	ENSP00000331327.5:n.1303+57T>G
ENST00000379077.9:c.*538+57T>G	ENSP00000368368.5:n.*538+57T>G
ENST00000379079.8:c.703+57T>G	ENSP00000368370.2:n.703+57T>G
ENST00000448076.9:c.1354+57T>G	ENSP00000413452.5:n.1354+57T>G
ENST00000452863.10:c.1354+57T>G MANE Select	ENSP00000415516.5:n.1354+57T>G
ENST00000526685.2:n.808+57T>G
ENST00000639563.3:c.1303+57T>G	ENSP00000492269.3:n.1303+57T>G
ENST00000639907.2:n.497+57T>G
ENST00000640146.2:c.679+57T>G	ENSP00000491984.2:n.679+57T>G
ENST00000650745.1:n.620T>G
ENST00000650861.1:n.1935+57T>G
ENST00000651459.1:c.125+57T>G
ENST00000651533.1:n.400+57T>G
ENST00000651668.1:n.291+57T>G
ENST00000651794.1:n.1197+57T>G
ENST00000651819.1:n.279+57T>G
ENST00000652579.1:n.614+57T>G
ENST00000652724.1:n.544+57T>G
ENST00000332351.7:c.1339+57T>G	ENSP00000331327.3:n.1339+57T>G
ENST00000379077.7:c.*538+57T>G	ENSP00000368368.3:n.*538+57T>G
ENST00000379079.6:c.703+57T>G	ENSP00000368370.2:n.703+57T>G
ENST00000448076.7:c.1339+57T>G	ENSP00000413452.3:n.1339+57T>G
ENST00000452863.7:c.1288+57T>G	ENSP00000415516.3:n.1288+57T>G
ENST00000527882.5:c.321-545T>G
ENST00000530998.5:c.652+57T>G	ENSP00000435307.1:n.652+57T>G
NM_000378.4:c.1288+57T>G	NP_000369.3:n.1288+57T>G
NM_001198551.1:c.703+57T>G , LRG_525t2:c.703+57T>G	NP_001185480.1:n.703+57T>G
NM_001198552.1:c.652+57T>G	NP_001185481.1:n.652+57T>G
NM_024424.3:c.1339+57T>G	NP_077742.2:n.1339+57T>G
NM_024426.4:c.1339+57T>G	NP_077744.3:n.1339+57T>G
NM_000378.5:c.1303+57T>G	NP_000369.4:n.1303+57T>G
NM_024424.4:c.1354+57T>G	NP_077742.3:n.1354+57T>G
NM_024426.5:c.1354+57T>G	NP_077744.4:n.1354+57T>G
NM_001367854.1:c.166+57T>G	NP_001354783.1:n.166+57T>G
NR_160306.1:n.1686+57T>G
NM_000378.6:c.1303+57T>G	NP_000369.4:n.1303+57T>G
NM_001198552.2:c.652+57T>G	NP_001185481.1:n.652+57T>G
NM_024424.5:c.1354+57T>G	NP_077742.3:n.1354+57T>G
NM_024426.6:c.1354+57T>G MANE Select	NP_077744.4:n.1354+57T>G