Canonical Allele Identifier: CA379959348

Gene: WT1

Linked Data

• MyVariant Identifiers: chr11:g.32414271T>G (hg19) ; chr11:g.32392725T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392725T>G , CM000673.2:g.32392725T>G	GRCh38
NC_000011.9:g.32414271T>G , CM000673.1:g.32414271T>G	GRCh37
NC_000011.8:g.32370847T>G	NCBI36
NG_009272.1:g.47817A>C , LRG_525:g.47817A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1244A>C	ENSP00000331327.5:p.Asp415Ala
ENST00000379077.9:c.*479A>C	ENSP00000368368.5:n.*479A>C
ENST00000379079.8:c.644A>C	ENSP00000368370.2:p.Asp215Ala
ENST00000448076.9:c.1295A>C	ENSP00000413452.5:p.Asp432Ala
ENST00000452863.10:c.1295A>C MANE Select	ENSP00000415516.5:p.Asp432Ala
ENST00000526685.2:n.749A>C
ENST00000639563.3:c.1244A>C	ENSP00000492269.3:p.Asp415Ala
ENST00000639907.2:n.438A>C
ENST00000640146.2:c.620A>C	ENSP00000491984.2:p.Asp207Ala
ENST00000650745.1:n.504A>C
ENST00000650861.1:n.1876A>C
ENST00000651459.1:c.66A>C
ENST00000651533.1:n.341A>C
ENST00000651668.1:n.232A>C
ENST00000651794.1:n.1138A>C
ENST00000651819.1:n.220A>C
ENST00000652579.1:n.555A>C
ENST00000652724.1:n.485A>C
ENST00000332351.7:c.1280A>C	ENSP00000331327.3:p.Asp427Ala
ENST00000379077.7:c.*479A>C	ENSP00000368368.3:n.*479A>C
ENST00000379079.6:c.644A>C	ENSP00000368370.2:p.Asp215Ala
ENST00000448076.7:c.1280A>C	ENSP00000413452.3:p.Asp427Ala
ENST00000452863.7:c.1229A>C	ENSP00000415516.3:p.Asp410Ala
ENST00000527882.5:c.321-661A>C
ENST00000530998.5:c.593A>C	ENSP00000435307.1:p.Asp198Ala
NM_000378.4:c.1229A>C	NP_000369.3:p.Asp410Ala
NM_001198551.1:c.644A>C , LRG_525t2:c.644A>C	NP_001185480.1:p.Asp215Ala
NM_001198552.1:c.593A>C	NP_001185481.1:p.Asp198Ala
NM_024424.3:c.1280A>C	NP_077742.2:p.Asp427Ala
NM_024426.4:c.1280A>C	NP_077744.3:p.Asp427Ala
NM_000378.5:c.1244A>C	NP_000369.4:p.Asp415Ala
NM_024424.4:c.1295A>C	NP_077742.3:p.Asp432Ala
NM_024426.5:c.1295A>C	NP_077744.4:p.Asp432Ala
NM_001367854.1:c.107A>C	NP_001354783.1:p.Asp36Ala
NR_160306.1:n.1627A>C
NM_000378.6:c.1244A>C	NP_000369.4:p.Asp415Ala
NM_001198552.2:c.593A>C	NP_001185481.1:p.Asp198Ala
NM_024424.5:c.1295A>C	NP_077742.3:p.Asp432Ala
NM_024426.6:c.1295A>C MANE Select	NP_077744.4:p.Asp432Ala