Canonical Allele Identifier: CA379963498

Gene: WT1

Linked Data

• ClinVar Variation Id: 476716
• ClinVar RCV Id: RCV000543084 ; RCV003459258 ; RCV003999466 ; RCV003228953
• dbSNP Id: rs1307992683
• gnomAD v2: 11-32450127-C-G
• gnomAD v4: 11-32428581-C-G
• MyVariant Identifiers: chr11:g.32450127C>G (hg19) ; chr11:g.32428581C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32428581C>G , CM000673.2:g.32428581C>G	GRCh38
NC_000011.9:g.32450127C>G , CM000673.1:g.32450127C>G	GRCh37
NC_000011.8:g.32406703C>G	NCBI36
NG_009272.1:g.11961G>C , LRG_525:g.11961G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.700G>C	ENSP00000331327.5:p.Gly234Arg
ENST00000379077.9:c.700G>C	ENSP00000368368.5:p.Gly234Arg
ENST00000379079.8:c.49G>C	ENSP00000368370.2:p.Gly17Arg
ENST00000448076.9:c.700G>C	ENSP00000413452.5:p.Gly234Arg
ENST00000452863.10:c.700G>C MANE Select	ENSP00000415516.5:p.Gly234Arg
ENST00000639563.3:c.700G>C	ENSP00000492269.3:p.Gly234Arg
ENST00000640146.2:c.76G>C	ENSP00000491984.2:p.Gly26Arg
ENST00000332351.7:c.685G>C	ENSP00000331327.3:p.Gly229Arg
ENST00000379077.7:c.685G>C	ENSP00000368368.3:p.Gly229Arg
ENST00000379079.6:c.49G>C	ENSP00000368370.2:p.Gly17Arg
ENST00000448076.7:c.685G>C	ENSP00000413452.3:p.Gly229Arg
ENST00000452863.7:c.685G>C	ENSP00000415516.3:p.Gly229Arg
ENST00000527775.1:c.-63G>C	ENSP00000435351.1:n.-63G>C
ENST00000530998.5:c.49G>C	ENSP00000435307.1:p.Gly17Arg
NM_000378.4:c.685G>C	NP_000369.3:p.Gly229Arg
NM_001198551.1:c.49G>C , LRG_525t2:c.49G>C	NP_001185480.1:p.Gly17Arg
NM_001198552.1:c.49G>C	NP_001185481.1:p.Gly17Arg
NM_024424.3:c.685G>C	NP_077742.2:p.Gly229Arg
NM_024426.4:c.685G>C	NP_077744.3:p.Gly229Arg
NM_000378.5:c.700G>C	NP_000369.4:p.Gly234Arg
NM_024424.4:c.700G>C	NP_077742.3:p.Gly234Arg
NM_024426.5:c.700G>C	NP_077744.4:p.Gly234Arg
NR_160306.1:n.879G>C
NM_000378.6:c.700G>C	NP_000369.4:p.Gly234Arg
NM_001198552.2:c.49G>C	NP_001185481.1:p.Gly17Arg
NM_024424.5:c.700G>C	NP_077742.3:p.Gly234Arg
NM_024426.6:c.700G>C MANE Select	NP_077744.4:p.Gly234Arg