Canonical Allele Identifier: CA219503835

Gene: WT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32428706dup , CM000673.2:g.32428706dup	GRCh38
NC_000011.9:g.32450252dup , CM000673.1:g.32450252dup	GRCh37
NC_000011.8:g.32406828dup	NCBI36
NG_009272.1:g.11843dup , LRG_525:g.11843dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.662-80dup	ENSP00000331327.5:n.662-80dup
ENST00000379077.9:c.662-80dup	ENSP00000368368.5:n.662-80dup
ENST00000379079.8:c.11-80dup	ENSP00000368370.2:n.11-80dup
ENST00000448076.9:c.662-80dup	ENSP00000413452.5:n.662-80dup
ENST00000452863.10:c.662-80dup MANE Select	ENSP00000415516.5:n.662-80dup
ENST00000639563.3:c.662-80dup	ENSP00000492269.3:n.662-80dup
ENST00000640146.2:c.38-80dup	ENSP00000491984.2:n.38-80dup
ENST00000332351.7:c.647-80dup	ENSP00000331327.3:n.647-80dup
ENST00000379077.7:c.647-80dup	ENSP00000368368.3:n.647-80dup
ENST00000379079.6:c.11-80dup	ENSP00000368370.2:n.11-80dup
ENST00000448076.7:c.647-80dup	ENSP00000413452.3:n.647-80dup
ENST00000452863.7:c.647-80dup	ENSP00000415516.3:n.647-80dup
ENST00000527775.1:c.-101-80dup	ENSP00000435351.1:n.-101-80dup
ENST00000530998.5:c.11-80dup	ENSP00000435307.1:n.11-80dup
NM_000378.4:c.647-80dup	NP_000369.3:n.647-80dup
NM_001198551.1:c.11-80dup , LRG_525t2:c.11-80dup	NP_001185480.1:n.11-80dup
NM_001198552.1:c.11-80dup	NP_001185481.1:n.11-80dup
NM_024424.3:c.647-80dup	NP_077742.2:n.647-80dup
NM_024426.4:c.647-80dup	NP_077744.3:n.647-80dup
NM_000378.5:c.662-80dup	NP_000369.4:n.662-80dup
NM_024424.4:c.662-80dup	NP_077742.3:n.662-80dup
NM_024426.5:c.662-80dup	NP_077744.4:n.662-80dup
NR_160306.1:n.841-80dup
NM_000378.6:c.662-80dup	NP_000369.4:n.662-80dup
NM_001198552.2:c.11-80dup	NP_001185481.1:n.11-80dup
NM_024424.5:c.662-80dup	NP_077742.3:n.662-80dup
NM_024426.6:c.662-80dup MANE Select	NP_077744.4:n.662-80dup