Canonical Allele Identifier: CA473565897

Gene: WT1

Linked Data

• ClinVar Variation Id: 2943881
• ClinVar RCV Id: RCV003803439
• dbSNP Id: rs2132921015
• MyVariant Identifiers: chr11:g.32414273C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392727C>T , CM000673.2:g.32392727C>T	GRCh38
NC_000011.9:g.32414273C>T , CM000673.1:g.32414273C>T	GRCh37
NC_000011.8:g.32370849C>T	NCBI36
NG_009272.1:g.47815G>A , LRG_525:g.47815G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1242G>A	ENSP00000331327.5:p.Lys414=
ENST00000379077.9:c.*477G>A	ENSP00000368368.5:n.*477G>A
ENST00000379079.8:c.642G>A	ENSP00000368370.2:p.Lys214=
ENST00000448076.9:c.1293G>A	ENSP00000413452.5:p.Lys431=
ENST00000452863.10:c.1293G>A MANE Select	ENSP00000415516.5:p.Lys431=
ENST00000526685.2:n.747G>A
ENST00000639563.3:c.1242G>A	ENSP00000492269.3:p.Lys414=
ENST00000639907.2:n.436G>A
ENST00000640146.2:c.618G>A	ENSP00000491984.2:p.Lys206=
ENST00000650745.1:n.502G>A
ENST00000650861.1:n.1874G>A
ENST00000651459.1:c.64G>A
ENST00000651533.1:n.339G>A
ENST00000651668.1:n.230G>A
ENST00000651794.1:n.1136G>A
ENST00000651819.1:n.218G>A
ENST00000652579.1:n.553G>A
ENST00000652724.1:n.483G>A
ENST00000332351.7:c.1278G>A	ENSP00000331327.3:p.Lys426=
ENST00000379077.7:c.*477G>A	ENSP00000368368.3:n.*477G>A
ENST00000379079.6:c.642G>A	ENSP00000368370.2:p.Lys214=
ENST00000448076.7:c.1278G>A	ENSP00000413452.3:p.Lys426=
ENST00000452863.7:c.1227G>A	ENSP00000415516.3:p.Lys409=
ENST00000527882.5:c.321-663G>A
ENST00000530998.5:c.591G>A	ENSP00000435307.1:p.Lys197=
NM_000378.4:c.1227G>A	NP_000369.3:p.Lys409=
NM_001198551.1:c.642G>A , LRG_525t2:c.642G>A	NP_001185480.1:p.Lys214=
NM_001198552.1:c.591G>A	NP_001185481.1:p.Lys197=
NM_024424.3:c.1278G>A	NP_077742.2:p.Lys426=
NM_024426.4:c.1278G>A	NP_077744.3:p.Lys426=
NM_000378.5:c.1242G>A	NP_000369.4:p.Lys414=
NM_024424.4:c.1293G>A	NP_077742.3:p.Lys431=
NM_024426.5:c.1293G>A	NP_077744.4:p.Lys431=
NM_001367854.1:c.105G>A	NP_001354783.1:p.Lys35=
NR_160306.1:n.1625G>A
NM_000378.6:c.1242G>A	NP_000369.4:p.Lys414=
NM_001198552.2:c.591G>A	NP_001185481.1:p.Lys197=
NM_024424.5:c.1293G>A	NP_077742.3:p.Lys431=
NM_024426.6:c.1293G>A MANE Select	NP_077744.4:p.Lys431=