Canonical Allele Identifier: CA379958911

Gene: WT1

Linked Data

• ClinVar Variation Id: 2681776
• ClinVar RCV Id: RCV003985900
• dbSNP Id: rs2132914929
• MyVariant Identifiers: chr11:g.32413581G>A (hg19) ; chr11:g.32392035G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392035G>A , CM000673.2:g.32392035G>A	GRCh38
NC_000011.9:g.32413581G>A , CM000673.1:g.32413581G>A	GRCh37
NC_000011.8:g.32370157G>A	NCBI36
NG_009272.1:g.48507C>T , LRG_525:g.48507C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1333C>T	ENSP00000331327.5:p.Gln445Ter
ENST00000379077.9:c.*568C>T	ENSP00000368368.5:n.*568C>T
ENST00000379079.8:c.733C>T	ENSP00000368370.2:p.Gln245Ter
ENST00000448076.9:c.1384C>T	ENSP00000413452.5:p.Gln462Ter
ENST00000452863.10:c.1384C>T MANE Select	ENSP00000415516.5:p.Gln462Ter
ENST00000526685.2:n.838C>T
ENST00000639563.3:c.1333C>T	ENSP00000492269.3:p.Gln445Ter
ENST00000639907.2:n.527C>T
ENST00000640146.2:c.709C>T	ENSP00000491984.2:p.Gln237Ter
ENST00000650745.1:n.1194C>T
ENST00000650861.1:n.1965C>T
ENST00000650986.1:n.47C>T
ENST00000651459.1:c.155C>T
ENST00000651533.1:n.430C>T
ENST00000651668.1:n.321C>T
ENST00000651794.1:n.1227C>T
ENST00000651819.1:n.309C>T
ENST00000652579.1:n.644C>T
ENST00000652724.1:n.574C>T
ENST00000332351.7:c.1369C>T	ENSP00000331327.3:p.Gln457Ter
ENST00000379077.7:c.*568C>T	ENSP00000368368.3:n.*568C>T
ENST00000379079.6:c.733C>T	ENSP00000368370.2:p.Gln245Ter
ENST00000448076.7:c.1369C>T	ENSP00000413452.3:p.Gln457Ter
ENST00000452863.7:c.1318C>T	ENSP00000415516.3:p.Gln440Ter
ENST00000527882.5:c.350C>T
ENST00000530998.5:c.682C>T	ENSP00000435307.1:p.Gln228Ter
NM_000378.4:c.1318C>T	NP_000369.3:p.Gln440Ter
NM_001198551.1:c.733C>T , LRG_525t2:c.733C>T	NP_001185480.1:p.Gln245Ter
NM_001198552.1:c.682C>T	NP_001185481.1:p.Gln228Ter
NM_024424.3:c.1369C>T	NP_077742.2:p.Gln457Ter
NM_024426.4:c.1369C>T	NP_077744.3:p.Gln457Ter
NM_000378.5:c.1333C>T	NP_000369.4:p.Gln445Ter
NM_024424.4:c.1384C>T	NP_077742.3:p.Gln462Ter
NM_024426.5:c.1384C>T	NP_077744.4:p.Gln462Ter
NM_001367854.1:c.196C>T	NP_001354783.1:p.Gln66Ter
NR_160306.1:n.1716C>T
NM_000378.6:c.1333C>T	NP_000369.4:p.Gln445Ter
NM_001198552.2:c.682C>T	NP_001185481.1:p.Gln228Ter
NM_024424.5:c.1384C>T	NP_077742.3:p.Gln462Ter
NM_024426.6:c.1384C>T MANE Select	NP_077744.4:p.Gln462Ter