Canonical Allele Identifier: CA379959131

Gene: WT1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1297C>A	ENSP00000331327.5:p.His433Asn
ENST00000379077.9:c.*532C>A	ENSP00000368368.5:n.*532C>A
ENST00000379079.8:c.697C>A	ENSP00000368370.2:p.His233Asn
ENST00000448076.9:c.1348C>A	ENSP00000413452.5:p.His450Asn
ENST00000452863.10:c.1348C>A MANE Select	ENSP00000415516.5:p.His450Asn
ENST00000526685.2:n.802C>A
ENST00000639563.3:c.1297C>A	ENSP00000492269.3:p.His433Asn
ENST00000639907.2:n.491C>A
ENST00000640146.2:c.673C>A	ENSP00000491984.2:p.His225Asn
ENST00000650745.1:n.557C>A
ENST00000650861.1:n.1929C>A
ENST00000651459.1:c.119C>A
ENST00000651533.1:n.394C>A
ENST00000651668.1:n.285C>A
ENST00000651794.1:n.1191C>A
ENST00000651819.1:n.273C>A
ENST00000652579.1:n.608C>A
ENST00000652724.1:n.538C>A
ENST00000332351.7:c.1333C>A	ENSP00000331327.3:p.His445Asn
ENST00000379077.7:c.*532C>A	ENSP00000368368.3:n.*532C>A
ENST00000379079.6:c.697C>A	ENSP00000368370.2:p.His233Asn
ENST00000448076.7:c.1333C>A	ENSP00000413452.3:p.His445Asn
ENST00000452863.7:c.1282C>A	ENSP00000415516.3:p.His428Asn
ENST00000527882.5:c.321-608C>A
ENST00000530998.5:c.646C>A	ENSP00000435307.1:p.His216Asn
NM_000378.4:c.1282C>A	NP_000369.3:p.His428Asn
NM_001198551.1:c.697C>A , LRG_525t2:c.697C>A	NP_001185480.1:p.His233Asn
NM_001198552.1:c.646C>A	NP_001185481.1:p.His216Asn
NM_024424.3:c.1333C>A	NP_077742.2:p.His445Asn
NM_024426.4:c.1333C>A	NP_077744.3:p.His445Asn
NM_000378.5:c.1297C>A	NP_000369.4:p.His433Asn
NM_024424.4:c.1348C>A	NP_077742.3:p.His450Asn
NM_024426.5:c.1348C>A	NP_077744.4:p.His450Asn
NM_001367854.1:c.160C>A	NP_001354783.1:p.His54Asn
NR_160306.1:n.1680C>A
NM_000378.6:c.1297C>A	NP_000369.4:p.His433Asn
NM_001198552.2:c.646C>A	NP_001185481.1:p.His216Asn
NM_024424.5:c.1348C>A	NP_077742.3:p.His450Asn
NM_024426.6:c.1348C>A MANE Select	NP_077744.4:p.His450Asn