Canonical Allele Identifier: CA379959178

Gene: WT1

Linked Data

• MyVariant Identifiers: chr11:g.32414232C>A (hg19) ; chr11:g.32392686C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392686C>A , CM000673.2:g.32392686C>A	GRCh38
NC_000011.9:g.32414232C>A , CM000673.1:g.32414232C>A	GRCh37
NC_000011.8:g.32370808C>A	NCBI36
NG_009272.1:g.47856G>T , LRG_525:g.47856G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1283G>T	ENSP00000331327.5:p.Arg428Ile
ENST00000379077.9:c.*518G>T	ENSP00000368368.5:n.*518G>T
ENST00000379079.8:c.683G>T	ENSP00000368370.2:p.Arg228Ile
ENST00000448076.9:c.1334G>T	ENSP00000413452.5:p.Arg445Ile
ENST00000452863.10:c.1334G>T MANE Select	ENSP00000415516.5:p.Arg445Ile
ENST00000526685.2:n.788G>T
ENST00000639563.3:c.1283G>T	ENSP00000492269.3:p.Arg428Ile
ENST00000639907.2:n.477G>T
ENST00000640146.2:c.659G>T	ENSP00000491984.2:p.Arg220Ile
ENST00000650745.1:n.543G>T
ENST00000650861.1:n.1915G>T
ENST00000651459.1:c.105G>T
ENST00000651533.1:n.380G>T
ENST00000651668.1:n.271G>T
ENST00000651794.1:n.1177G>T
ENST00000651819.1:n.259G>T
ENST00000652579.1:n.594G>T
ENST00000652724.1:n.524G>T
ENST00000332351.7:c.1319G>T	ENSP00000331327.3:p.Arg440Ile
ENST00000379077.7:c.*518G>T	ENSP00000368368.3:n.*518G>T
ENST00000379079.6:c.683G>T	ENSP00000368370.2:p.Arg228Ile
ENST00000448076.7:c.1319G>T	ENSP00000413452.3:p.Arg440Ile
ENST00000452863.7:c.1268G>T	ENSP00000415516.3:p.Arg423Ile
ENST00000527882.5:c.321-622G>T
ENST00000530998.5:c.632G>T	ENSP00000435307.1:p.Arg211Ile
NM_000378.4:c.1268G>T	NP_000369.3:p.Arg423Ile
NM_001198551.1:c.683G>T , LRG_525t2:c.683G>T	NP_001185480.1:p.Arg228Ile
NM_001198552.1:c.632G>T	NP_001185481.1:p.Arg211Ile
NM_024424.3:c.1319G>T	NP_077742.2:p.Arg440Ile
NM_024426.4:c.1319G>T	NP_077744.3:p.Arg440Ile
NM_000378.5:c.1283G>T	NP_000369.4:p.Arg428Ile
NM_024424.4:c.1334G>T	NP_077742.3:p.Arg445Ile
NM_024426.5:c.1334G>T	NP_077744.4:p.Arg445Ile
NM_001367854.1:c.146G>T	NP_001354783.1:p.Arg49Ile
NR_160306.1:n.1666G>T
NM_000378.6:c.1283G>T	NP_000369.4:p.Arg428Ile
NM_001198552.2:c.632G>T	NP_001185481.1:p.Arg211Ile
NM_024424.5:c.1334G>T	NP_077742.3:p.Arg445Ile
NM_024426.6:c.1334G>T MANE Select	NP_077744.4:p.Arg445Ile