Canonical Allele Identifier: CA2612971927

Gene: WT1

Linked Data

• gnomAD v4: 11-32388886-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32388886T>C , CM000673.2:g.32388886T>C	GRCh38
NC_000011.9:g.32410432T>C , CM000673.1:g.32410432T>C	GRCh37
NC_000011.8:g.32367008T>C	NCBI36
NG_009272.1:g.51656A>G , LRG_525:g.51656A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.*172A>G	ENSP00000331327.5:n.*172A>G
ENST00000379077.9:c.*925A>G	ENSP00000368368.5:n.*925A>G
ENST00000379079.8:c.*172A>G	ENSP00000368370.2:n.*172A>G
ENST00000448076.9:c.*172A>G	ENSP00000413452.5:n.*172A>G
ENST00000452863.10:c.*172A>G MANE Select	ENSP00000415516.5:n.*172A>G
ENST00000639907.2:n.875A>G
ENST00000640146.2:c.*172A>G	ENSP00000491984.2:n.*172A>G
ENST00000650745.1:n.1551A>G
ENST00000650861.1:n.2313A>G
ENST00000651459.1:c.512A>G
ENST00000651533.1:n.778A>G
ENST00000651668.1:n.678A>G
ENST00000651794.1:n.1584A>G
ENST00000651819.1:n.666A>G
ENST00000652579.1:n.1001A>G
ENST00000652724.1:n.931A>G
ENST00000332351.7:c.*172A>G	ENSP00000331327.3:n.*172A>G
ENST00000379077.7:c.*925A>G	ENSP00000368368.3:n.*925A>G
ENST00000379079.6:c.*172A>G	ENSP00000368370.2:n.*172A>G
ENST00000448076.7:c.*172A>G	ENSP00000413452.3:n.*172A>G
ENST00000452863.7:c.1666A>G	ENSP00000415516.3:n.1666A>G
ENST00000530998.5:c.*172A>G	ENSP00000435307.1:n.*172A>G
NM_000378.4:c.*172A>G	NP_000369.3:n.*172A>G
NM_001198551.1:c.*172A>G , LRG_525t2:c.*172A>G	NP_001185480.1:n.*172A>G
NM_001198552.1:c.*172A>G	NP_001185481.1:n.*172A>G
NM_024424.3:c.*172A>G	NP_077742.2:n.*172A>G
NM_024426.4:c.*172A>G	NP_077744.3:n.*172A>G
NM_000378.5:c.*172A>G	NP_000369.4:n.*172A>G
NM_024424.4:c.*172A>G	NP_077742.3:n.*172A>G
NM_024426.5:c.*172A>G	NP_077744.4:n.*172A>G
NM_001367854.1:c.*172A>G	NP_001354783.1:n.*172A>G
NR_160306.1:n.2073A>G
NM_000378.6:c.*172A>G	NP_000369.4:n.*172A>G
NM_001198552.2:c.*172A>G	NP_001185481.1:n.*172A>G
NM_024424.5:c.*172A>G	NP_077742.3:n.*172A>G
NM_024426.6:c.*172A>G MANE Select	NP_077744.4:n.*172A>G