Canonical Allele Identifier: CA675632527

Gene: WT1

Linked Data

• dbSNP Id: rs1312517834
• gnomAD v3: 11-32392518-A-G
• gnomAD v4: 11-32392518-A-G
• MyVariant Identifiers: chr11:g.32414064A>G (hg19) ; chr11:g.32392518A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392518A>G , CM000673.2:g.32392518A>G	GRCh38
NC_000011.9:g.32414064A>G , CM000673.1:g.32414064A>G	GRCh37
NC_000011.8:g.32370640A>G	NCBI36
NG_009272.1:g.48024T>C , LRG_525:g.48024T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1303+148T>C	ENSP00000331327.5:n.1303+148T>C
ENST00000379077.9:c.*538+148T>C	ENSP00000368368.5:n.*538+148T>C
ENST00000379079.8:c.703+148T>C	ENSP00000368370.2:n.703+148T>C
ENST00000448076.9:c.1354+148T>C	ENSP00000413452.5:n.1354+148T>C
ENST00000452863.10:c.1354+148T>C MANE Select	ENSP00000415516.5:n.1354+148T>C
ENST00000526685.2:n.808+148T>C
ENST00000639563.3:c.1303+148T>C	ENSP00000492269.3:n.1303+148T>C
ENST00000639907.2:n.497+148T>C
ENST00000640146.2:c.679+148T>C	ENSP00000491984.2:n.679+148T>C
ENST00000650745.1:n.711T>C
ENST00000650861.1:n.1935+148T>C
ENST00000651459.1:c.125+148T>C
ENST00000651533.1:n.400+148T>C
ENST00000651668.1:n.291+148T>C
ENST00000651794.1:n.1197+148T>C
ENST00000651819.1:n.279+148T>C
ENST00000652579.1:n.614+148T>C
ENST00000652724.1:n.544+148T>C
ENST00000332351.7:c.1339+148T>C	ENSP00000331327.3:n.1339+148T>C
ENST00000379077.7:c.*538+148T>C	ENSP00000368368.3:n.*538+148T>C
ENST00000379079.6:c.703+148T>C	ENSP00000368370.2:n.703+148T>C
ENST00000448076.7:c.1339+148T>C	ENSP00000413452.3:n.1339+148T>C
ENST00000452863.7:c.1288+148T>C	ENSP00000415516.3:n.1288+148T>C
ENST00000527882.5:c.321-454T>C
ENST00000530998.5:c.652+148T>C	ENSP00000435307.1:n.652+148T>C
NM_000378.4:c.1288+148T>C	NP_000369.3:n.1288+148T>C
NM_001198551.1:c.703+148T>C , LRG_525t2:c.703+148T>C	NP_001185480.1:n.703+148T>C
NM_001198552.1:c.652+148T>C	NP_001185481.1:n.652+148T>C
NM_024424.3:c.1339+148T>C	NP_077742.2:n.1339+148T>C
NM_024426.4:c.1339+148T>C	NP_077744.3:n.1339+148T>C
NM_000378.5:c.1303+148T>C	NP_000369.4:n.1303+148T>C
NM_024424.4:c.1354+148T>C	NP_077742.3:n.1354+148T>C
NM_024426.5:c.1354+148T>C	NP_077744.4:n.1354+148T>C
NM_001367854.1:c.166+148T>C	NP_001354783.1:n.166+148T>C
NR_160306.1:n.1686+148T>C
NM_000378.6:c.1303+148T>C	NP_000369.4:n.1303+148T>C
NM_001198552.2:c.652+148T>C	NP_001185481.1:n.652+148T>C
NM_024424.5:c.1354+148T>C	NP_077742.3:n.1354+148T>C
NM_024426.6:c.1354+148T>C MANE Select	NP_077744.4:n.1354+148T>C