Canonical Allele Identifier: CA379964944

Gene: WT1

Linked Data

• ClinVar Variation Id: 543125
• ClinVar RCV Id: RCV000653788
• dbSNP Id: rs1554946500
• MyVariant Identifiers: chr11:g.32456429G>A (hg19) ; chr11:g.32434883G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32434883G>A , CM000673.2:g.32434883G>A	GRCh38
NC_000011.9:g.32456429G>A , CM000673.1:g.32456429G>A	GRCh37
NC_000011.8:g.32413005G>A	NCBI36
NG_009272.1:g.5659C>T , LRG_525:g.5659C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.478C>T	ENSP00000331327.5:p.Gln160Ter
ENST00000379077.9:c.478C>T	ENSP00000368368.5:p.Gln160Ter
ENST00000448076.9:c.478C>T	ENSP00000413452.5:p.Gln160Ter
ENST00000452863.10:c.478C>T MANE Select	ENSP00000415516.5:p.Gln160Ter
ENST00000639563.3:c.478C>T	ENSP00000492269.3:p.Gln160Ter
ENST00000332351.7:c.463C>T	ENSP00000331327.3:p.Gln155Ter
ENST00000379077.7:c.463C>T	ENSP00000368368.3:p.Gln155Ter
ENST00000448076.7:c.463C>T	ENSP00000413452.3:p.Gln155Ter
ENST00000452863.7:c.463C>T	ENSP00000415516.3:p.Gln155Ter
NM_000378.4:c.463C>T	NP_000369.3:p.Gln155Ter
NM_024424.3:c.463C>T	NP_077742.2:p.Gln155Ter
NM_024426.4:c.463C>T	NP_077744.3:p.Gln155Ter
NM_000378.5:c.478C>T	NP_000369.4:p.Gln160Ter
NM_024424.4:c.478C>T	NP_077742.3:p.Gln160Ter
NM_024426.5:c.478C>T	NP_077744.4:p.Gln160Ter
NR_160306.1:n.657C>T
NM_000378.6:c.478C>T	NP_000369.4:p.Gln160Ter
NM_024424.5:c.478C>T	NP_077742.3:p.Gln160Ter
NM_024426.6:c.478C>T MANE Select	NP_077744.4:p.Gln160Ter