Canonical Allele Identifier: CA473568319

Gene: WT1

Linked Data

• dbSNP Id: rs2133037265
• MyVariant Identifiers: chr11:g.32439164G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32417618G>A , CM000673.2:g.32417618G>A	GRCh38
NC_000011.9:g.32439164G>A , CM000673.1:g.32439164G>A	GRCh37
NC_000011.8:g.32395740G>A	NCBI36
NG_009272.1:g.22924C>T , LRG_525:g.22924C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.924C>T	ENSP00000331327.5:p.Cys308=
ENST00000379077.9:c.924C>T	ENSP00000368368.5:p.Cys308=
ENST00000379079.8:c.273C>T	ENSP00000368370.2:p.Cys91=
ENST00000448076.9:c.924C>T	ENSP00000413452.5:p.Cys308=
ENST00000452863.10:c.924C>T MANE Select	ENSP00000415516.5:p.Cys308=
ENST00000639563.3:c.924C>T	ENSP00000492269.3:p.Cys308=
ENST00000640146.2:c.300C>T	ENSP00000491984.2:p.Cys100=
ENST00000332351.7:c.909C>T	ENSP00000331327.3:p.Cys303=
ENST00000379077.7:c.909C>T	ENSP00000368368.3:p.Cys303=
ENST00000379079.6:c.273C>T	ENSP00000368370.2:p.Cys91=
ENST00000448076.7:c.909C>T	ENSP00000413452.3:p.Cys303=
ENST00000452863.7:c.909C>T	ENSP00000415516.3:p.Cys303=
ENST00000527775.1:c.162C>T	ENSP00000435351.1:p.Cys54=
ENST00000530998.5:c.273C>T	ENSP00000435307.1:p.Cys91=
NM_000378.4:c.909C>T	NP_000369.3:p.Cys303=
NM_001198551.1:c.273C>T , LRG_525t2:c.273C>T	NP_001185480.1:p.Cys91=
NM_001198552.1:c.273C>T	NP_001185481.1:p.Cys91=
NM_024424.3:c.909C>T	NP_077742.2:p.Cys303=
NM_024426.4:c.909C>T	NP_077744.3:p.Cys303=
NM_000378.5:c.924C>T	NP_000369.4:p.Cys308=
NM_024424.4:c.924C>T	NP_077742.3:p.Cys308=
NM_024426.5:c.924C>T	NP_077744.4:p.Cys308=
NR_160306.1:n.1103C>T
NM_000378.6:c.924C>T	NP_000369.4:p.Cys308=
NM_001198552.2:c.273C>T	NP_001185481.1:p.Cys91=
NM_024424.5:c.924C>T	NP_077742.3:p.Cys308=
NM_024426.6:c.924C>T MANE Select	NP_077744.4:p.Cys308=