Canonical Allele Identifier: CA15702872

Gene: WT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32416356G>A , CM000673.2:g.32416356G>A	GRCh38
NC_000011.9:g.32437902G>A , CM000673.1:g.32437902G>A	GRCh37
NC_000011.8:g.32394478G>A	NCBI36
NG_009272.1:g.24186C>T , LRG_525:g.24186C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_024426.6:c.1016+134C>T MANE Select	NP_077744.4:n.1016+134C>T
ENST00000452863.10:c.1016+134C>T MANE Select	ENSP00000415516.5:n.1016+134C>T
NM_000378.4:c.950+1221C>T	NP_000369.3:n.950+1221C>T
NM_000378.5:c.965+1221C>T	NP_000369.4:n.965+1221C>T
NM_000378.6:c.965+1221C>T	NP_000369.4:n.965+1221C>T
NM_001198551.1:c.365+134C>T , LRG_525t2:c.365+134C>T	NP_001185480.1:n.365+134C>T
NM_001198552.1:c.314+1221C>T	NP_001185481.1:n.314+1221C>T
NM_001198552.2:c.314+1221C>T	NP_001185481.1:n.314+1221C>T
NM_024424.3:c.1001+134C>T	NP_077742.2:n.1001+134C>T
NM_024424.4:c.1016+134C>T	NP_077742.3:n.1016+134C>T
NM_024424.5:c.1016+134C>T	NP_077742.3:n.1016+134C>T
NM_024426.4:c.1001+134C>T	NP_077744.3:n.1001+134C>T
NM_024426.5:c.1016+134C>T	NP_077744.4:n.1016+134C>T
NR_160306.1:n.1348+134C>T
ENST00000332351.7:c.1001+134C>T	ENSP00000331327.3:n.1001+134C>T
ENST00000332351.9:c.965+1221C>T	ENSP00000331327.5:n.965+1221C>T
ENST00000379077.7:c.*200+134C>T	ENSP00000368368.3:n.*200+134C>T
ENST00000379077.9:c.*200+134C>T	ENSP00000368368.5:n.*200+134C>T
ENST00000379079.6:c.365+134C>T	ENSP00000368370.2:n.365+134C>T
ENST00000379079.8:c.365+134C>T	ENSP00000368370.2:n.365+134C>T
ENST00000448076.7:c.1001+134C>T	ENSP00000413452.3:n.1001+134C>T
ENST00000448076.9:c.1016+134C>T	ENSP00000413452.5:n.1016+134C>T
ENST00000452863.7:c.950+1221C>T	ENSP00000415516.3:n.950+1221C>T
ENST00000527775.1:c.254+134C>T	ENSP00000435351.1:n.254+134C>T
ENST00000527882.5:c.72+134C>T
ENST00000530998.5:c.314+1221C>T	ENSP00000435307.1:n.314+1221C>T
ENST00000639563.3:c.965+1221C>T	ENSP00000492269.3:n.965+1221C>T
ENST00000640146.2:c.341+1221C>T	ENSP00000491984.2:n.341+1221C>T
ENST00000651794.1:n.759+134C>T