Canonical Allele Identifier: CA379963272

Gene: WT1

Linked Data

• ClinVar Variation Id: 1041600
• ClinVar RCV Id: RCV001345427
• dbSNP Id: rs1853140429
• MyVariant Identifiers: chr11:g.32450053C>G (hg19) ; chr11:g.32428507C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32428507C>G , CM000673.2:g.32428507C>G	GRCh38
NC_000011.9:g.32450053C>G , CM000673.1:g.32450053C>G	GRCh37
NC_000011.8:g.32406629C>G	NCBI36
NG_009272.1:g.12035G>C , LRG_525:g.12035G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.774G>C	ENSP00000331327.5:p.Gln258His
ENST00000379077.9:c.774G>C	ENSP00000368368.5:p.Gln258His
ENST00000379079.8:c.123G>C	ENSP00000368370.2:p.Gln41His
ENST00000448076.9:c.774G>C	ENSP00000413452.5:p.Gln258His
ENST00000452863.10:c.774G>C MANE Select	ENSP00000415516.5:p.Gln258His
ENST00000639563.3:c.774G>C	ENSP00000492269.3:p.Gln258His
ENST00000640146.2:c.150G>C	ENSP00000491984.2:p.Gln50His
ENST00000332351.7:c.759G>C	ENSP00000331327.3:p.Gln253His
ENST00000379077.7:c.759G>C	ENSP00000368368.3:p.Gln253His
ENST00000379079.6:c.123G>C	ENSP00000368370.2:p.Gln41His
ENST00000448076.7:c.759G>C	ENSP00000413452.3:p.Gln253His
ENST00000452863.7:c.759G>C	ENSP00000415516.3:p.Gln253His
ENST00000527775.1:c.12G>C	ENSP00000435351.1:p.Gln4His
ENST00000530998.5:c.123G>C	ENSP00000435307.1:p.Gln41His
NM_000378.4:c.759G>C	NP_000369.3:p.Gln253His
NM_001198551.1:c.123G>C , LRG_525t2:c.123G>C	NP_001185480.1:p.Gln41His
NM_001198552.1:c.123G>C	NP_001185481.1:p.Gln41His
NM_024424.3:c.759G>C	NP_077742.2:p.Gln253His
NM_024426.4:c.759G>C	NP_077744.3:p.Gln253His
NM_000378.5:c.774G>C	NP_000369.4:p.Gln258His
NM_024424.4:c.774G>C	NP_077742.3:p.Gln258His
NM_024426.5:c.774G>C	NP_077744.4:p.Gln258His
NR_160306.1:n.953G>C
NM_000378.6:c.774G>C	NP_000369.4:p.Gln258His
NM_001198552.2:c.123G>C	NP_001185481.1:p.Gln41His
NM_024424.5:c.774G>C	NP_077742.3:p.Gln258His
NM_024426.6:c.774G>C MANE Select	NP_077744.4:p.Gln258His