Canonical Allele Identifier: CA379962176

Gene: WT1

Linked Data

• ClinVar Variation Id: 2946654
• ClinVar RCV Id: RCV003808892
• dbSNP Id: rs1852719405
• MyVariant Identifiers: chr11:g.32439180G>A (hg19) ; chr11:g.32417634G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32417634G>A , CM000673.2:g.32417634G>A	GRCh38
NC_000011.9:g.32439180G>A , CM000673.1:g.32439180G>A	GRCh37
NC_000011.8:g.32395756G>A	NCBI36
NG_009272.1:g.22908C>T , LRG_525:g.22908C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.908C>T	ENSP00000331327.5:p.Thr303Ile
ENST00000379077.9:c.908C>T	ENSP00000368368.5:p.Thr303Ile
ENST00000379079.8:c.257C>T	ENSP00000368370.2:p.Thr86Ile
ENST00000448076.9:c.908C>T	ENSP00000413452.5:p.Thr303Ile
ENST00000452863.10:c.908C>T MANE Select	ENSP00000415516.5:p.Thr303Ile
ENST00000639563.3:c.908C>T	ENSP00000492269.3:p.Thr303Ile
ENST00000640146.2:c.284C>T	ENSP00000491984.2:p.Thr95Ile
ENST00000332351.7:c.893C>T	ENSP00000331327.3:p.Thr298Ile
ENST00000379077.7:c.893C>T	ENSP00000368368.3:p.Thr298Ile
ENST00000379079.6:c.257C>T	ENSP00000368370.2:p.Thr86Ile
ENST00000448076.7:c.893C>T	ENSP00000413452.3:p.Thr298Ile
ENST00000452863.7:c.893C>T	ENSP00000415516.3:p.Thr298Ile
ENST00000527775.1:c.146C>T	ENSP00000435351.1:p.Thr49Ile
ENST00000530998.5:c.257C>T	ENSP00000435307.1:p.Thr86Ile
NM_000378.4:c.893C>T	NP_000369.3:p.Thr298Ile
NM_001198551.1:c.257C>T , LRG_525t2:c.257C>T	NP_001185480.1:p.Thr86Ile
NM_001198552.1:c.257C>T	NP_001185481.1:p.Thr86Ile
NM_024424.3:c.893C>T	NP_077742.2:p.Thr298Ile
NM_024426.4:c.893C>T	NP_077744.3:p.Thr298Ile
NM_000378.5:c.908C>T	NP_000369.4:p.Thr303Ile
NM_024424.4:c.908C>T	NP_077742.3:p.Thr303Ile
NM_024426.5:c.908C>T	NP_077744.4:p.Thr303Ile
NR_160306.1:n.1087C>T
NM_000378.6:c.908C>T	NP_000369.4:p.Thr303Ile
NM_001198552.2:c.257C>T	NP_001185481.1:p.Thr86Ile
NM_024424.5:c.908C>T	NP_077742.3:p.Thr303Ile
NM_024426.6:c.908C>T MANE Select	NP_077744.4:p.Thr303Ile