Canonical Allele Identifier: CA2790961094

Gene: WT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392034_32392035insAAAAAAAAAAA , CM000673.2:g.32392034_32392035insAAAAAAAAAAA	GRCh38
NC_000011.9:g.32413580_32413581insAAAAAAAAAAA , CM000673.1:g.32413580_32413581insAAAAAAAAAAA	GRCh37
NC_000011.8:g.32370156_32370157insAAAAAAAAAAA	NCBI36
NG_009272.1:g.48507_48508insTTTTTTTTTTT , LRG_525:g.48507_48508insTTTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1333_1334insTTTTTTTTTTT	ENSP00000331327.5:p.Gln445LeufsTer14
ENST00000379077.9:c.*568_*569insTTTTTTTTTTT	ENSP00000368368.5:n.*568_*569insTTTTTTTTTTT
ENST00000379079.8:c.733_734insTTTTTTTTTTT	ENSP00000368370.2:p.Gln245LeufsTer14
ENST00000448076.9:c.1384_1385insTTTTTTTTTTT	ENSP00000413452.5:p.Gln462LeufsTer14
ENST00000452863.10:c.1384_1385insTTTTTTTTTTT MANE Select	ENSP00000415516.5:p.Gln462LeufsTer14
ENST00000526685.2:n.838_839insTTTTTTTTTTT
ENST00000639563.3:c.1333_1334insTTTTTTTTTTT	ENSP00000492269.3:p.Gln445LeufsTer14
ENST00000639907.2:n.527_528insTTTTTTTTTTT
ENST00000640146.2:c.709_710insTTTTTTTTTTT	ENSP00000491984.2:p.Gln237LeufsTer14
ENST00000650745.1:n.1194_1195insTTTTTTTTTTT
ENST00000650861.1:n.1965_1966insTTTTTTTTTTT
ENST00000650986.1:n.47_48insTTTTTTTTTTT
ENST00000651459.1:c.155_156insTTTTTTTTTTT
ENST00000651533.1:n.430_431insTTTTTTTTTTT
ENST00000651668.1:n.321_322insTTTTTTTTTTT
ENST00000651794.1:n.1227_1228insTTTTTTTTTTT
ENST00000651819.1:n.309_310insTTTTTTTTTTT
ENST00000652579.1:n.644_645insTTTTTTTTTTT
ENST00000652724.1:n.574_575insTTTTTTTTTTT
ENST00000332351.7:c.1369_1370insTTTTTTTTTTT	ENSP00000331327.3:p.Gln457LeufsTer14
ENST00000379077.7:c.*568_*569insTTTTTTTTTTT	ENSP00000368368.3:n.*568_*569insTTTTTTTTTTT
ENST00000379079.6:c.733_734insTTTTTTTTTTT	ENSP00000368370.2:p.Gln245LeufsTer14
ENST00000448076.7:c.1369_1370insTTTTTTTTTTT	ENSP00000413452.3:p.Gln457LeufsTer14
ENST00000452863.7:c.1318_1319insTTTTTTTTTTT	ENSP00000415516.3:p.Gln440LeufsTer14
ENST00000527882.5:c.350_351insTTTTTTTTTTT
ENST00000530998.5:c.682_683insTTTTTTTTTTT	ENSP00000435307.1:p.Gln228LeufsTer14
NM_000378.4:c.1318_1319insTTTTTTTTTTT	NP_000369.3:p.Gln440LeufsTer14
NM_001198551.1:c.733_734insTTTTTTTTTTT , LRG_525t2:c.733_734insTTTTTTTTTTT	NP_001185480.1:p.Gln245LeufsTer14
NM_001198552.1:c.682_683insTTTTTTTTTTT	NP_001185481.1:p.Gln228LeufsTer14
NM_024424.3:c.1369_1370insTTTTTTTTTTT	NP_077742.2:p.Gln457LeufsTer14
NM_024426.4:c.1369_1370insTTTTTTTTTTT	NP_077744.3:p.Gln457LeufsTer14
NM_000378.5:c.1333_1334insTTTTTTTTTTT	NP_000369.4:p.Gln445LeufsTer14
NM_024424.4:c.1384_1385insTTTTTTTTTTT	NP_077742.3:p.Gln462LeufsTer14
NM_024426.5:c.1384_1385insTTTTTTTTTTT	NP_077744.4:p.Gln462LeufsTer14
NM_001367854.1:c.196_197insTTTTTTTTTTT	NP_001354783.1:p.Gln66LeufsTer14
NR_160306.1:n.1716_1717insTTTTTTTTTTT
NM_000378.6:c.1333_1334insTTTTTTTTTTT	NP_000369.4:p.Gln445LeufsTer14
NM_001198552.2:c.682_683insTTTTTTTTTTT	NP_001185481.1:p.Gln228LeufsTer14
NM_024424.5:c.1384_1385insTTTTTTTTTTT	NP_077742.3:p.Gln462LeufsTer14
NM_024426.6:c.1384_1385insTTTTTTTTTTT MANE Select	NP_077744.4:p.Gln462LeufsTer14