Canonical Allele Identifier: CA473773434

Gene: WT1

Linked Data

• ClinVar Variation Id: 1077951
• ClinVar RCV Id: RCV001392712
• dbSNP Id: rs1590411695
• gnomAD v4: 11-32435310-C-G
• MyVariant Identifiers: chr11:g.32456856C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32435310C>G , CM000673.2:g.32435310C>G	GRCh38
NC_000011.9:g.32456856C>G , CM000673.1:g.32456856C>G	GRCh37
NC_000011.8:g.32413432C>G	NCBI36
NG_009272.1:g.5232G>C , LRG_525:g.5232G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.51G>C	ENSP00000331327.5:p.Pro17=
ENST00000379077.9:c.51G>C	ENSP00000368368.5:p.Pro17=
ENST00000448076.9:c.51G>C	ENSP00000413452.5:p.Pro17=
ENST00000452863.10:c.51G>C MANE Select	ENSP00000415516.5:p.Pro17=
ENST00000639563.3:c.51G>C	ENSP00000492269.3:p.Pro17=
ENST00000332351.7:c.36G>C	ENSP00000331327.3:p.Pro12=
ENST00000379077.7:c.36G>C	ENSP00000368368.3:p.Pro12=
ENST00000448076.7:c.36G>C	ENSP00000413452.3:p.Pro12=
ENST00000452863.7:c.36G>C	ENSP00000415516.3:p.Pro12=
NM_000378.4:c.36G>C	NP_000369.3:p.Pro12=
NM_024424.3:c.36G>C	NP_077742.2:p.Pro12=
NM_024426.4:c.36G>C	NP_077744.3:p.Pro12=
NM_000378.5:c.51G>C	NP_000369.4:p.Pro17=
NM_024424.4:c.51G>C	NP_077742.3:p.Pro17=
NM_024426.5:c.51G>C	NP_077744.4:p.Pro17=
NR_160306.1:n.230G>C
NM_000378.6:c.51G>C	NP_000369.4:p.Pro17=
NM_024424.5:c.51G>C	NP_077742.3:p.Pro17=
NM_024426.6:c.51G>C MANE Select	NP_077744.4:p.Pro17=