Canonical Allele Identifier: CA645577705

Gene: WT1

Linked Data

• COSMIC: COSM5944605

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32417646_32417647insTTA , CM000673.2:g.32417646_32417647insTTA	GRCh38
NC_000011.9:g.32439192_32439193insTTA , CM000673.1:g.32439192_32439193insTTA	GRCh37
NC_000011.8:g.32395768_32395769insTTA	NCBI36
NG_009272.1:g.22897_22898insATA , LRG_525:g.22897_22898insATA

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.897_898insATA	ENSP00000331327.5:p.Leu299_Tyr300insIle
ENST00000379077.9:c.897_898insATA	ENSP00000368368.5:p.Leu299_Tyr300insIle
ENST00000379079.8:c.246_247insATA	ENSP00000368370.2:p.Leu82_Tyr83insIle
ENST00000448076.9:c.897_898insATA	ENSP00000413452.5:p.Leu299_Tyr300insIle
ENST00000452863.10:c.897_898insATA MANE Select	ENSP00000415516.5:p.Leu299_Tyr300insIle
ENST00000639563.3:c.897_898insATA	ENSP00000492269.3:p.Leu299_Tyr300insIle
ENST00000640146.2:c.273_274insATA	ENSP00000491984.2:p.Leu91_Tyr92insIle
ENST00000332351.7:c.882_883insATA	ENSP00000331327.3:p.Leu294_Tyr295insIle
ENST00000379077.7:c.882_883insATA	ENSP00000368368.3:p.Leu294_Tyr295insIle
ENST00000379079.6:c.246_247insATA	ENSP00000368370.2:p.Leu82_Tyr83insIle
ENST00000448076.7:c.882_883insATA	ENSP00000413452.3:p.Leu294_Tyr295insIle
ENST00000452863.7:c.882_883insATA	ENSP00000415516.3:p.Leu294_Tyr295insIle
ENST00000527775.1:c.135_136insATA	ENSP00000435351.1:p.Leu45_Tyr46insIle
ENST00000530998.5:c.246_247insATA	ENSP00000435307.1:p.Leu82_Tyr83insIle
NM_000378.4:c.882_883insATA	NP_000369.3:p.Leu294_Tyr295insIle
NM_001198551.1:c.246_247insATA , LRG_525t2:c.246_247insATA	NP_001185480.1:p.Leu82_Tyr83insIle
NM_001198552.1:c.246_247insATA	NP_001185481.1:p.Leu82_Tyr83insIle
NM_024424.3:c.882_883insATA	NP_077742.2:p.Leu294_Tyr295insIle
NM_024426.4:c.882_883insATA	NP_077744.3:p.Leu294_Tyr295insIle
NM_000378.5:c.897_898insATA	NP_000369.4:p.Leu299_Tyr300insIle
NM_024424.4:c.897_898insATA	NP_077742.3:p.Leu299_Tyr300insIle
NM_024426.5:c.897_898insATA	NP_077744.4:p.Leu299_Tyr300insIle
NR_160306.1:n.1076_1077insATA
NM_000378.6:c.897_898insATA	NP_000369.4:p.Leu299_Tyr300insIle
NM_001198552.2:c.246_247insATA	NP_001185481.1:p.Leu82_Tyr83insIle
NM_024424.5:c.897_898insATA	NP_077742.3:p.Leu299_Tyr300insIle
NM_024426.6:c.897_898insATA MANE Select	NP_077744.4:p.Leu299_Tyr300insIle