Canonical Allele Identifier: CA379958968

Gene: WT1

Linked Data

• dbSNP Id: rs546743811
• MyVariant Identifiers: chr11:g.32413594C>G (hg19) ; chr11:g.32392048C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392048C>G , CM000673.2:g.32392048C>G	GRCh38
NC_000011.9:g.32413594C>G , CM000673.1:g.32413594C>G	GRCh37
NC_000011.8:g.32370170C>G	NCBI36
NG_009272.1:g.48494G>C , LRG_525:g.48494G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1320G>C	ENSP00000331327.5:p.Gln440His
ENST00000379077.9:c.*555G>C	ENSP00000368368.5:n.*555G>C
ENST00000379079.8:c.720G>C	ENSP00000368370.2:p.Gln240His
ENST00000448076.9:c.1371G>C	ENSP00000413452.5:p.Gln457His
ENST00000452863.10:c.1371G>C MANE Select	ENSP00000415516.5:p.Gln457His
ENST00000526685.2:n.825G>C
ENST00000639563.3:c.1320G>C	ENSP00000492269.3:p.Gln440His
ENST00000639907.2:n.514G>C
ENST00000640146.2:c.696G>C	ENSP00000491984.2:p.Gln232His
ENST00000650745.1:n.1181G>C
ENST00000650861.1:n.1952G>C
ENST00000650986.1:n.34G>C
ENST00000651459.1:c.142G>C
ENST00000651533.1:n.417G>C
ENST00000651668.1:n.308G>C
ENST00000651794.1:n.1214G>C
ENST00000651819.1:n.296G>C
ENST00000652579.1:n.631G>C
ENST00000652724.1:n.561G>C
ENST00000332351.7:c.1356G>C	ENSP00000331327.3:p.Gln452His
ENST00000379077.7:c.*555G>C	ENSP00000368368.3:n.*555G>C
ENST00000379079.6:c.720G>C	ENSP00000368370.2:p.Gln240His
ENST00000448076.7:c.1356G>C	ENSP00000413452.3:p.Gln452His
ENST00000452863.7:c.1305G>C	ENSP00000415516.3:p.Gln435His
ENST00000527882.5:c.337G>C
ENST00000530998.5:c.669G>C	ENSP00000435307.1:p.Gln223His
NM_000378.4:c.1305G>C	NP_000369.3:p.Gln435His
NM_001198551.1:c.720G>C , LRG_525t2:c.720G>C	NP_001185480.1:p.Gln240His
NM_001198552.1:c.669G>C	NP_001185481.1:p.Gln223His
NM_024424.3:c.1356G>C	NP_077742.2:p.Gln452His
NM_024426.4:c.1356G>C	NP_077744.3:p.Gln452His
NM_000378.5:c.1320G>C	NP_000369.4:p.Gln440His
NM_024424.4:c.1371G>C	NP_077742.3:p.Gln457His
NM_024426.5:c.1371G>C	NP_077744.4:p.Gln457His
NM_001367854.1:c.183G>C	NP_001354783.1:p.Gln61His
NR_160306.1:n.1703G>C
NM_000378.6:c.1320G>C	NP_000369.4:p.Gln440His
NM_001198552.2:c.669G>C	NP_001185481.1:p.Gln223His
NM_024424.5:c.1371G>C	NP_077742.3:p.Gln457His
NM_024426.6:c.1371G>C MANE Select	NP_077744.4:p.Gln457His