Canonical Allele Identifier: CA658658038

Gene: WT1

Linked Data

• ClinVar Variation Id: 476713
• ClinVar RCV Id: RCV000541858
• dbSNP Id: rs1554945232
• MyVariant Identifiers: chr11:g.32450145dup (hg19) ; chr11:g.32428599dup (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32428599dup , CM000673.2:g.32428599dup	GRCh38
NC_000011.9:g.32450145dup , CM000673.1:g.32450145dup	GRCh37
NC_000011.8:g.32406721dup	NCBI36
NG_009272.1:g.11943dup , LRG_525:g.11943dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.682dup	ENSP00000331327.5:p.Asp228GlyfsTer25
ENST00000379077.9:c.682dup	ENSP00000368368.5:p.Asp228GlyfsTer25
ENST00000379079.8:c.31dup	ENSP00000368370.2:p.Asp11GlyfsTer25
ENST00000448076.9:c.682dup	ENSP00000413452.5:p.Asp228GlyfsTer25
ENST00000452863.10:c.682dup MANE Select	ENSP00000415516.5:p.Asp228GlyfsTer25
ENST00000639563.3:c.682dup	ENSP00000492269.3:p.Asp228GlyfsTer25
ENST00000640146.2:c.58dup	ENSP00000491984.2:p.Asp20GlyfsTer25
ENST00000332351.7:c.667dup	ENSP00000331327.3:p.Asp223GlyfsTer25
ENST00000379077.7:c.667dup	ENSP00000368368.3:p.Asp223GlyfsTer25
ENST00000379079.6:c.31dup	ENSP00000368370.2:p.Asp11GlyfsTer25
ENST00000448076.7:c.667dup	ENSP00000413452.3:p.Asp223GlyfsTer25
ENST00000452863.7:c.667dup	ENSP00000415516.3:p.Asp223GlyfsTer25
ENST00000527775.1:c.-81dup	ENSP00000435351.1:n.-81dup
ENST00000530998.5:c.31dup	ENSP00000435307.1:p.Asp11GlyfsTer25
NM_000378.4:c.667dup	NP_000369.3:p.Asp223GlyfsTer25
NM_001198551.1:c.31dup , LRG_525t2:c.31dup	NP_001185480.1:p.Asp11GlyfsTer25
NM_001198552.1:c.31dup	NP_001185481.1:p.Asp11GlyfsTer25
NM_024424.3:c.667dup	NP_077742.2:p.Asp223GlyfsTer25
NM_024426.4:c.667dup	NP_077744.3:p.Asp223GlyfsTer25
NM_000378.5:c.682dup	NP_000369.4:p.Asp228GlyfsTer25
NM_024424.4:c.682dup	NP_077742.3:p.Asp228GlyfsTer25
NM_024426.5:c.682dup	NP_077744.4:p.Asp228GlyfsTer25
NR_160306.1:n.861dup
NM_000378.6:c.682dup	NP_000369.4:p.Asp228GlyfsTer25
NM_001198552.2:c.31dup	NP_001185481.1:p.Asp11GlyfsTer25
NM_024424.5:c.682dup	NP_077742.3:p.Asp228GlyfsTer25
NM_024426.6:c.682dup MANE Select	NP_077744.4:p.Asp228GlyfsTer25