Canonical Allele Identifier: CA645577702

Gene: WT1

Linked Data

• COSMIC: COSM250070

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32417581_32417582dup , CM000673.2:g.32417581_32417582dup	GRCh38
NC_000011.9:g.32439127_32439128dup , CM000673.1:g.32439127_32439128dup	GRCh37
NC_000011.8:g.32395703_32395704dup	NCBI36
NG_009272.1:g.22961_22962dup , LRG_525:g.22961_22962dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.961_962dup	ENSP00000331327.5:p.Gly322ArgfsTer?
ENST00000379077.9:c.961_962dup	ENSP00000368368.5:p.Gly322ArgfsTer?
ENST00000379079.8:c.310_311dup	ENSP00000368370.2:p.Gly105ArgfsTer11
ENST00000448076.9:c.961_962dup	ENSP00000413452.5:p.Gly322ArgfsTer11
ENST00000452863.10:c.961_962dup MANE Select	ENSP00000415516.5:p.Gly322ArgfsTer11
ENST00000639563.3:c.961_962dup	ENSP00000492269.3:p.Gly322ArgfsTer?
ENST00000640146.2:c.337_338dup	ENSP00000491984.2:p.Gly114ArgfsTer?
ENST00000332351.7:c.946_947dup	ENSP00000331327.3:p.Gly317ArgfsTer11
ENST00000379077.7:c.946_947dup	ENSP00000368368.3:p.Gly317ArgfsTer?
ENST00000379079.6:c.310_311dup	ENSP00000368370.2:p.Gly105ArgfsTer11
ENST00000448076.7:c.946_947dup	ENSP00000413452.3:p.Gly317ArgfsTer11
ENST00000452863.7:c.946_947dup	ENSP00000415516.3:p.Gly317ArgfsTer?
ENST00000527775.1:c.199_200dup	ENSP00000435351.1:p.Gly68ArgfsTer11
ENST00000527882.5:c.17_18dup
ENST00000530998.5:c.310_311dup	ENSP00000435307.1:p.Gly105ArgfsTer?
NM_000378.4:c.946_947dup	NP_000369.3:p.Gly317ArgfsTer?
NM_001198551.1:c.310_311dup , LRG_525t2:c.310_311dup	NP_001185480.1:p.Gly105ArgfsTer11
NM_001198552.1:c.310_311dup	NP_001185481.1:p.Gly105ArgfsTer?
NM_024424.3:c.946_947dup	NP_077742.2:p.Gly317ArgfsTer11
NM_024426.4:c.946_947dup	NP_077744.3:p.Gly317ArgfsTer11
NM_000378.5:c.961_962dup	NP_000369.4:p.Gly322ArgfsTer?
NM_024424.4:c.961_962dup	NP_077742.3:p.Gly322ArgfsTer11
NM_024426.5:c.961_962dup	NP_077744.4:p.Gly322ArgfsTer11
NR_160306.1:n.1140_1141dup
NM_000378.6:c.961_962dup	NP_000369.4:p.Gly322ArgfsTer?
NM_001198552.2:c.310_311dup	NP_001185481.1:p.Gly105ArgfsTer?
NM_024424.5:c.961_962dup	NP_077742.3:p.Gly322ArgfsTer11
NM_024426.6:c.961_962dup MANE Select	NP_077744.4:p.Gly322ArgfsTer11