Canonical Allele Identifier: CA379963269

Gene: WT1

Linked Data

• COSMIC: COSM3666909 ; COSM3666910
• MyVariant Identifiers: chr11:g.32450052C>G (hg19) ; chr11:g.32428506C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32428506C>G , CM000673.2:g.32428506C>G	GRCh38
NC_000011.9:g.32450052C>G , CM000673.1:g.32450052C>G	GRCh37
NC_000011.8:g.32406628C>G	NCBI36
NG_009272.1:g.12036G>C , LRG_525:g.12036G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.775G>C	ENSP00000331327.5:p.Gly259Arg
ENST00000379077.9:c.775G>C	ENSP00000368368.5:p.Gly259Arg
ENST00000379079.8:c.124G>C	ENSP00000368370.2:p.Gly42Arg
ENST00000448076.9:c.775G>C	ENSP00000413452.5:p.Gly259Arg
ENST00000452863.10:c.775G>C MANE Select	ENSP00000415516.5:p.Gly259Arg
ENST00000639563.3:c.775G>C	ENSP00000492269.3:p.Gly259Arg
ENST00000640146.2:c.151G>C	ENSP00000491984.2:p.Gly51Arg
ENST00000332351.7:c.760G>C	ENSP00000331327.3:p.Gly254Arg
ENST00000379077.7:c.760G>C	ENSP00000368368.3:p.Gly254Arg
ENST00000379079.6:c.124G>C	ENSP00000368370.2:p.Gly42Arg
ENST00000448076.7:c.760G>C	ENSP00000413452.3:p.Gly254Arg
ENST00000452863.7:c.760G>C	ENSP00000415516.3:p.Gly254Arg
ENST00000527775.1:c.13G>C	ENSP00000435351.1:p.Gly5Arg
ENST00000530998.5:c.124G>C	ENSP00000435307.1:p.Gly42Arg
NM_000378.4:c.760G>C	NP_000369.3:p.Gly254Arg
NM_001198551.1:c.124G>C , LRG_525t2:c.124G>C	NP_001185480.1:p.Gly42Arg
NM_001198552.1:c.124G>C	NP_001185481.1:p.Gly42Arg
NM_024424.3:c.760G>C	NP_077742.2:p.Gly254Arg
NM_024426.4:c.760G>C	NP_077744.3:p.Gly254Arg
NM_000378.5:c.775G>C	NP_000369.4:p.Gly259Arg
NM_024424.4:c.775G>C	NP_077742.3:p.Gly259Arg
NM_024426.5:c.775G>C	NP_077744.4:p.Gly259Arg
NR_160306.1:n.954G>C
NM_000378.6:c.775G>C	NP_000369.4:p.Gly259Arg
NM_001198552.2:c.124G>C	NP_001185481.1:p.Gly42Arg
NM_024424.5:c.775G>C	NP_077742.3:p.Gly259Arg
NM_024426.6:c.775G>C MANE Select	NP_077744.4:p.Gly259Arg