Canonical Allele Identifier: CA064291
Community Standard Title: NM_024426.6(WT1):c.1141C>T (p.Pro381Ser)
Gene: WT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32396380G>A , CM000673.2:g.32396380G>A GRCh38
NC_000011.9:g.32417926G>A , CM000673.1:g.32417926G>A GRCh37
NC_000011.8:g.32374502G>A NCBI36
NG_009272.1:g.44162C>T , LRG_525:g.44162C>T

Transcript Alleles

HGVS Amino-acid Change
NM_024426.6:c.1141C>T MANE Select NP_077744.4:p.Pro381Ser
ENST00000452863.10:c.1141C>T MANE Select ENSP00000415516.5:p.Pro381Ser
NM_000378.4:c.1075C>T NP_000369.3:p.Pro359Ser
NM_000378.5:c.1090C>T NP_000369.4:p.Pro364Ser
NM_000378.6:c.1090C>T NP_000369.4:p.Pro364Ser
NM_001198551.1:c.490C>T , LRG_525t2:c.490C>T NP_001185480.1:p.Pro164Ser
NM_001198552.1:c.439C>T NP_001185481.1:p.Pro147Ser
NM_001198552.2:c.439C>T NP_001185481.1:p.Pro147Ser
NM_001367854.1:c.-48C>T NP_001354783.1:n.-48C>T
NM_024424.3:c.1126C>T NP_077742.2:p.Pro376Ser
NM_024424.4:c.1141C>T NP_077742.3:p.Pro381Ser
NM_024424.5:c.1141C>T NP_077742.3:p.Pro381Ser
NM_024426.4:c.1126C>T NP_077744.3:p.Pro376Ser
NM_024426.5:c.1141C>T NP_077744.4:p.Pro381Ser
NR_160306.1:n.1473C>T
ENST00000332351.7:c.1126C>T ENSP00000331327.3:p.Pro376Ser
ENST00000332351.9:c.1090C>T ENSP00000331327.5:p.Pro364Ser
ENST00000379077.7:c.*325C>T ENSP00000368368.3:n.*325C>T
ENST00000379077.9:c.*325C>T ENSP00000368368.5:n.*325C>T
ENST00000379079.6:c.490C>T ENSP00000368370.2:p.Pro164Ser
ENST00000379079.8:c.490C>T ENSP00000368370.2:p.Pro164Ser
ENST00000448076.7:c.1126C>T ENSP00000413452.3:p.Pro376Ser
ENST00000448076.9:c.1141C>T ENSP00000413452.5:p.Pro381Ser
ENST00000452863.7:c.1075C>T ENSP00000415516.3:p.Pro359Ser
ENST00000526685.1:c.-48C>T ENSP00000436292.1:n.-48C>T
ENST00000526685.2:n.595C>T
ENST00000527775.1:c.379C>T ENSP00000435351.1:p.Pro127Ser
ENST00000527882.5:c.197C>T
ENST00000530998.5:c.439C>T ENSP00000435307.1:p.Pro147Ser
ENST00000639563.3:c.1090C>T ENSP00000492269.3:p.Pro364Ser
ENST00000639907.2:n.284C>T
ENST00000640146.2:c.466C>T ENSP00000491984.2:p.Pro156Ser
ENST00000650861.1:n.1722C>T
ENST00000651459.1:c.35+3568C>T
ENST00000651668.1:n.78C>T
ENST00000651794.1:n.884C>T
ENST00000651819.1:n.66C>T
ENST00000652579.1:n.301C>T
ENST00000652724.1:n.331C>T