Canonical Allele Identifier: CA379959129

Gene: WT1

Linked Data

• dbSNP Id: rs28942089
• MyVariant Identifiers: chr11:g.32414218G>C (hg19) ; chr11:g.32392672G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392672G>C , CM000673.2:g.32392672G>C	GRCh38
NC_000011.9:g.32414218G>C , CM000673.1:g.32414218G>C	GRCh37
NC_000011.8:g.32370794G>C	NCBI36
NG_009272.1:g.47870C>G , LRG_525:g.47870C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1297C>G	ENSP00000331327.5:p.His433Asp
ENST00000379077.9:c.*532C>G	ENSP00000368368.5:n.*532C>G
ENST00000379079.8:c.697C>G	ENSP00000368370.2:p.His233Asp
ENST00000448076.9:c.1348C>G	ENSP00000413452.5:p.His450Asp
ENST00000452863.10:c.1348C>G MANE Select	ENSP00000415516.5:p.His450Asp
ENST00000526685.2:n.802C>G
ENST00000639563.3:c.1297C>G	ENSP00000492269.3:p.His433Asp
ENST00000639907.2:n.491C>G
ENST00000640146.2:c.673C>G	ENSP00000491984.2:p.His225Asp
ENST00000650745.1:n.557C>G
ENST00000650861.1:n.1929C>G
ENST00000651459.1:c.119C>G
ENST00000651533.1:n.394C>G
ENST00000651668.1:n.285C>G
ENST00000651794.1:n.1191C>G
ENST00000651819.1:n.273C>G
ENST00000652579.1:n.608C>G
ENST00000652724.1:n.538C>G
ENST00000332351.7:c.1333C>G	ENSP00000331327.3:p.His445Asp
ENST00000379077.7:c.*532C>G	ENSP00000368368.3:n.*532C>G
ENST00000379079.6:c.697C>G	ENSP00000368370.2:p.His233Asp
ENST00000448076.7:c.1333C>G	ENSP00000413452.3:p.His445Asp
ENST00000452863.7:c.1282C>G	ENSP00000415516.3:p.His428Asp
ENST00000527882.5:c.321-608C>G
ENST00000530998.5:c.646C>G	ENSP00000435307.1:p.His216Asp
NM_000378.4:c.1282C>G	NP_000369.3:p.His428Asp
NM_001198551.1:c.697C>G , LRG_525t2:c.697C>G	NP_001185480.1:p.His233Asp
NM_001198552.1:c.646C>G	NP_001185481.1:p.His216Asp
NM_024424.3:c.1333C>G	NP_077742.2:p.His445Asp
NM_024426.4:c.1333C>G	NP_077744.3:p.His445Asp
NM_000378.5:c.1297C>G	NP_000369.4:p.His433Asp
NM_024424.4:c.1348C>G	NP_077742.3:p.His450Asp
NM_024426.5:c.1348C>G	NP_077744.4:p.His450Asp
NM_001367854.1:c.160C>G	NP_001354783.1:p.His54Asp
NR_160306.1:n.1680C>G
NM_000378.6:c.1297C>G	NP_000369.4:p.His433Asp
NM_001198552.2:c.646C>G	NP_001185481.1:p.His216Asp
NM_024424.5:c.1348C>G	NP_077742.3:p.His450Asp
NM_024426.6:c.1348C>G MANE Select	NP_077744.4:p.His450Asp