Canonical Allele Identifier: CA379966152
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1397701
ClinVar RCV Id: RCV001922394
dbSNP Id: rs1392405207

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32435150G>A , CM000673.2:g.32435150G>A GRCh38
NC_000011.9:g.32456696G>A , CM000673.1:g.32456696G>A GRCh37
NC_000011.8:g.32413272G>A NCBI36
NG_009272.1:g.5392C>T , LRG_525:g.5392C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000332351.9:c.211C>T ENSP00000331327.5:p.Pro71Ser
ENST00000379077.9:c.211C>T ENSP00000368368.5:p.Pro71Ser
ENST00000448076.9:c.211C>T ENSP00000413452.5:p.Pro71Ser
ENST00000452863.10:c.211C>T MANE Select ENSP00000415516.5:p.Pro71Ser
ENST00000639563.3:c.211C>T ENSP00000492269.3:p.Pro71Ser
ENST00000332351.7:c.196C>T ENSP00000331327.3:p.Pro66Ser
ENST00000379077.7:c.196C>T ENSP00000368368.3:p.Pro66Ser
ENST00000448076.7:c.196C>T ENSP00000413452.3:p.Pro66Ser
ENST00000452863.7:c.196C>T ENSP00000415516.3:p.Pro66Ser
NM_000378.4:c.196C>T NP_000369.3:p.Pro66Ser
NM_024424.3:c.196C>T NP_077742.2:p.Pro66Ser
NM_024426.4:c.196C>T NP_077744.3:p.Pro66Ser
NM_000378.5:c.211C>T NP_000369.4:p.Pro71Ser
NM_024424.4:c.211C>T NP_077742.3:p.Pro71Ser
NM_024426.5:c.211C>T NP_077744.4:p.Pro71Ser
NR_160306.1:n.390C>T
NM_000378.6:c.211C>T NP_000369.4:p.Pro71Ser
NM_024424.5:c.211C>T NP_077742.3:p.Pro71Ser
NM_024426.6:c.211C>T MANE Select NP_077744.4:p.Pro71Ser