Canonical Allele Identifier: CA473565281

Gene: WT1

Linked Data

• gnomAD v4: 11-32391988-A-G
• MyVariant Identifiers: chr11:g.32413534A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32391988A>G , CM000673.2:g.32391988A>G	GRCh38
NC_000011.9:g.32413534A>G , CM000673.1:g.32413534A>G	GRCh37
NC_000011.8:g.32370110A>G	NCBI36
NG_009272.1:g.48554T>C , LRG_525:g.48554T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1380T>C	ENSP00000331327.5:p.Thr460=
ENST00000379077.9:c.*615T>C	ENSP00000368368.5:n.*615T>C
ENST00000379079.8:c.780T>C	ENSP00000368370.2:p.Thr260=
ENST00000448076.9:c.1431T>C	ENSP00000413452.5:p.Thr477=
ENST00000452863.10:c.1431T>C MANE Select	ENSP00000415516.5:p.Thr477=
ENST00000526685.2:n.885T>C
ENST00000639563.3:c.1380T>C	ENSP00000492269.3:p.Thr460=
ENST00000639907.2:n.574T>C
ENST00000640146.2:c.756T>C	ENSP00000491984.2:p.Thr252=
ENST00000650745.1:n.1241T>C
ENST00000650861.1:n.2012T>C
ENST00000650986.1:n.94T>C
ENST00000651459.1:c.202T>C
ENST00000651533.1:n.477T>C
ENST00000651668.1:n.368T>C
ENST00000651794.1:n.1274T>C
ENST00000651819.1:n.356T>C
ENST00000652579.1:n.691T>C
ENST00000652724.1:n.621T>C
ENST00000332351.7:c.1416T>C	ENSP00000331327.3:p.Thr472=
ENST00000379077.7:c.*615T>C	ENSP00000368368.3:n.*615T>C
ENST00000379079.6:c.780T>C	ENSP00000368370.2:p.Thr260=
ENST00000448076.7:c.1416T>C	ENSP00000413452.3:p.Thr472=
ENST00000452863.7:c.1365T>C	ENSP00000415516.3:p.Thr455=
ENST00000527882.5:c.397T>C
ENST00000530998.5:c.729T>C	ENSP00000435307.1:p.Thr243=
NM_000378.4:c.1365T>C	NP_000369.3:p.Thr455=
NM_001198551.1:c.780T>C , LRG_525t2:c.780T>C	NP_001185480.1:p.Thr260=
NM_001198552.1:c.729T>C	NP_001185481.1:p.Thr243=
NM_024424.3:c.1416T>C	NP_077742.2:p.Thr472=
NM_024426.4:c.1416T>C	NP_077744.3:p.Thr472=
NM_000378.5:c.1380T>C	NP_000369.4:p.Thr460=
NM_024424.4:c.1431T>C	NP_077742.3:p.Thr477=
NM_024426.5:c.1431T>C	NP_077744.4:p.Thr477=
NM_001367854.1:c.243T>C	NP_001354783.1:p.Thr81=
NR_160306.1:n.1763T>C
NM_000378.6:c.1380T>C	NP_000369.4:p.Thr460=
NM_001198552.2:c.729T>C	NP_001185481.1:p.Thr243=
NM_024424.5:c.1431T>C	NP_077742.3:p.Thr477=
NM_024426.6:c.1431T>C MANE Select	NP_077744.4:p.Thr477=