Canonical Allele Identifier: CA1962340754

Gene: WT1

Linked Data

• dbSNP Id: rs1852114348

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32400263_32400267dup , CM000673.2:g.32400263_32400267dup	GRCh38
NC_000011.9:g.32421809_32421813dup , CM000673.1:g.32421809_32421813dup	GRCh37
NC_000011.8:g.32378385_32378389dup	NCBI36
NG_009272.1:g.40276_40280dup , LRG_525:g.40276_40280dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.966-222_966-218dup	ENSP00000331327.5:n.966-222_966-218dup
ENST00000379077.9:c.*201-222_*201-218dup	ENSP00000368368.5:n.*201-222_*201-218dup
ENST00000379079.8:c.366-222_366-218dup	ENSP00000368370.2:n.366-222_366-218dup
ENST00000448076.9:c.1017-222_1017-218dup	ENSP00000413452.5:n.1017-222_1017-218dup
ENST00000452863.10:c.1017-222_1017-218dup MANE Select	ENSP00000415516.5:n.1017-222_1017-218dup
ENST00000526685.2:n.350_354dup
ENST00000639563.3:c.966-222_966-218dup	ENSP00000492269.3:n.966-222_966-218dup
ENST00000640146.2:c.342-222_342-218dup	ENSP00000491984.2:n.342-222_342-218dup
ENST00000651794.1:n.760-222_760-218dup
ENST00000652579.1:n.177-222_177-218dup
ENST00000652724.1:n.86_90dup
ENST00000332351.7:c.1002-222_1002-218dup	ENSP00000331327.3:n.1002-222_1002-218dup
ENST00000379077.7:c.*201-222_*201-218dup	ENSP00000368368.3:n.*201-222_*201-218dup
ENST00000379079.6:c.366-222_366-218dup	ENSP00000368370.2:n.366-222_366-218dup
ENST00000448076.7:c.1002-222_1002-218dup	ENSP00000413452.3:n.1002-222_1002-218dup
ENST00000452863.7:c.951-222_951-218dup	ENSP00000415516.3:n.951-222_951-218dup
ENST00000526685.1:c.-293_-289dup	ENSP00000436292.1:n.-293_-289dup
ENST00000527775.1:c.255-222_255-218dup	ENSP00000435351.1:n.255-222_255-218dup
ENST00000527882.5:c.73-222_73-218dup
ENST00000530998.5:c.315-222_315-218dup	ENSP00000435307.1:n.315-222_315-218dup
NM_000378.4:c.951-222_951-218dup	NP_000369.3:n.951-222_951-218dup
NM_001198551.1:c.366-222_366-218dup , LRG_525t2:c.366-222_366-218dup	NP_001185480.1:n.366-222_366-218dup
NM_001198552.1:c.315-222_315-218dup	NP_001185481.1:n.315-222_315-218dup
NM_024424.3:c.1002-222_1002-218dup	NP_077742.2:n.1002-222_1002-218dup
NM_024426.4:c.1002-222_1002-218dup	NP_077744.3:n.1002-222_1002-218dup
NM_000378.5:c.966-222_966-218dup	NP_000369.4:n.966-222_966-218dup
NM_024424.4:c.1017-222_1017-218dup	NP_077742.3:n.1017-222_1017-218dup
NM_024426.5:c.1017-222_1017-218dup	NP_077744.4:n.1017-222_1017-218dup
NM_001367854.1:c.-293_-289dup	NP_001354783.1:n.-293_-289dup
NR_160306.1:n.1349-222_1349-218dup
NM_000378.6:c.966-222_966-218dup	NP_000369.4:n.966-222_966-218dup
NM_001198552.2:c.315-222_315-218dup	NP_001185481.1:n.315-222_315-218dup
NM_024424.5:c.1017-222_1017-218dup	NP_077742.3:n.1017-222_1017-218dup
NM_024426.6:c.1017-222_1017-218dup MANE Select	NP_077744.4:n.1017-222_1017-218dup