Canonical Allele Identifier: CA379966255

Gene: WT1

Linked Data

• ClinVar Variation Id: 2093007
• ClinVar RCV Id: RCV003008350
• MyVariant Identifiers: chr11:g.32456746C>G (hg19) ; chr11:g.32435200C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32435200C>G , CM000673.2:g.32435200C>G	GRCh38
NC_000011.9:g.32456746C>G , CM000673.1:g.32456746C>G	GRCh37
NC_000011.8:g.32413322C>G	NCBI36
NG_009272.1:g.5342G>C , LRG_525:g.5342G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.161G>C	ENSP00000331327.5:p.Ser54Thr
ENST00000379077.9:c.161G>C	ENSP00000368368.5:p.Ser54Thr
ENST00000448076.9:c.161G>C	ENSP00000413452.5:p.Ser54Thr
ENST00000452863.10:c.161G>C MANE Select	ENSP00000415516.5:p.Ser54Thr
ENST00000639563.3:c.161G>C	ENSP00000492269.3:p.Ser54Thr
ENST00000332351.7:c.146G>C	ENSP00000331327.3:p.Ser49Thr
ENST00000379077.7:c.146G>C	ENSP00000368368.3:p.Ser49Thr
ENST00000448076.7:c.146G>C	ENSP00000413452.3:p.Ser49Thr
ENST00000452863.7:c.146G>C	ENSP00000415516.3:p.Ser49Thr
NM_000378.4:c.146G>C	NP_000369.3:p.Ser49Thr
NM_024424.3:c.146G>C	NP_077742.2:p.Ser49Thr
NM_024426.4:c.146G>C	NP_077744.3:p.Ser49Thr
NM_000378.5:c.161G>C	NP_000369.4:p.Ser54Thr
NM_024424.4:c.161G>C	NP_077742.3:p.Ser54Thr
NM_024426.5:c.161G>C	NP_077744.4:p.Ser54Thr
NR_160306.1:n.340G>C
NM_000378.6:c.161G>C	NP_000369.4:p.Ser54Thr
NM_024424.5:c.161G>C	NP_077742.3:p.Ser54Thr
NM_024426.6:c.161G>C MANE Select	NP_077744.4:p.Ser54Thr