Canonical Allele Identifier: CA379959427

Gene: WT1

Linked Data

• MyVariant Identifiers: chr11:g.32414293G>T (hg19) ; chr11:g.32392747G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392747G>T , CM000673.2:g.32392747G>T	GRCh38
NC_000011.9:g.32414293G>T , CM000673.1:g.32414293G>T	GRCh37
NC_000011.8:g.32370869G>T	NCBI36
NG_009272.1:g.47795C>A , LRG_525:g.47795C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1222C>A	ENSP00000331327.5:p.Pro408Thr
ENST00000379077.9:c.*457C>A	ENSP00000368368.5:n.*457C>A
ENST00000379079.8:c.622C>A	ENSP00000368370.2:p.Pro208Thr
ENST00000448076.9:c.1273C>A	ENSP00000413452.5:p.Pro425Thr
ENST00000452863.10:c.1273C>A MANE Select	ENSP00000415516.5:p.Pro425Thr
ENST00000526685.2:n.727C>A
ENST00000639563.3:c.1222C>A	ENSP00000492269.3:p.Pro408Thr
ENST00000639907.2:n.416C>A
ENST00000640146.2:c.598C>A	ENSP00000491984.2:p.Pro200Thr
ENST00000650745.1:n.482C>A
ENST00000650861.1:n.1854C>A
ENST00000651459.1:c.44C>A
ENST00000651533.1:n.319C>A
ENST00000651668.1:n.210C>A
ENST00000651794.1:n.1116C>A
ENST00000651819.1:n.198C>A
ENST00000652579.1:n.533C>A
ENST00000652724.1:n.463C>A
ENST00000332351.7:c.1258C>A	ENSP00000331327.3:p.Pro420Thr
ENST00000379077.7:c.*457C>A	ENSP00000368368.3:n.*457C>A
ENST00000379079.6:c.622C>A	ENSP00000368370.2:p.Pro208Thr
ENST00000448076.7:c.1258C>A	ENSP00000413452.3:p.Pro420Thr
ENST00000452863.7:c.1207C>A	ENSP00000415516.3:p.Pro403Thr
ENST00000527882.5:c.321-683C>A
ENST00000530998.5:c.571C>A	ENSP00000435307.1:p.Pro191Thr
NM_000378.4:c.1207C>A	NP_000369.3:p.Pro403Thr
NM_001198551.1:c.622C>A , LRG_525t2:c.622C>A	NP_001185480.1:p.Pro208Thr
NM_001198552.1:c.571C>A	NP_001185481.1:p.Pro191Thr
NM_024424.3:c.1258C>A	NP_077742.2:p.Pro420Thr
NM_024426.4:c.1258C>A	NP_077744.3:p.Pro420Thr
NM_000378.5:c.1222C>A	NP_000369.4:p.Pro408Thr
NM_024424.4:c.1273C>A	NP_077742.3:p.Pro425Thr
NM_024426.5:c.1273C>A	NP_077744.4:p.Pro425Thr
NM_001367854.1:c.85C>A	NP_001354783.1:p.Pro29Thr
NR_160306.1:n.1605C>A
NM_000378.6:c.1222C>A	NP_000369.4:p.Pro408Thr
NM_001198552.2:c.571C>A	NP_001185481.1:p.Pro191Thr
NM_024424.5:c.1273C>A	NP_077742.3:p.Pro425Thr
NM_024426.6:c.1273C>A MANE Select	NP_077744.4:p.Pro425Thr