Canonical Allele Identifier: CA10634642

Gene: WT1

Linked Data

• ClinVar Variation Id: 304390
• ClinVar RCV Id: RCV000278661 ; RCV000343075 ; RCV000403928
• dbSNP Id: rs1042347
• gnomAD v2: 11-32409784-C-G
• gnomAD v3: 11-32388238-C-G
• gnomAD v4: 11-32388238-C-G
• MyVariant Identifiers: chr11:g.32409784C>G (hg19) ; chr11:g.32388238C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32388238C>G , CM000673.2:g.32388238C>G	GRCh38
NC_000011.9:g.32409784C>G , CM000673.1:g.32409784C>G	GRCh37
NC_000011.8:g.32366360C>G	NCBI36
NG_009272.1:g.52304G>C , LRG_525:g.52304G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.*820G>C	ENSP00000331327.5:n.*820G>C
ENST00000379077.9:c.*1573G>C	ENSP00000368368.5:n.*1573G>C
ENST00000379079.8:c.*820G>C	ENSP00000368370.2:n.*820G>C
ENST00000452863.10:c.*820G>C MANE Select	ENSP00000415516.5:n.*820G>C
ENST00000639907.2:n.1523G>C
ENST00000640146.2:c.*820G>C	ENSP00000491984.2:n.*820G>C
ENST00000650745.1:n.2199G>C
ENST00000650861.1:n.2961G>C
ENST00000651533.1:n.1426G>C
ENST00000651668.1:n.1326G>C
ENST00000651794.1:n.2232G>C
ENST00000651819.1:n.1314G>C
ENST00000652579.1:n.1649G>C
ENST00000652724.1:n.1579G>C
ENST00000332351.7:c.*820G>C	ENSP00000331327.3:n.*820G>C
ENST00000379077.7:c.*1573G>C	ENSP00000368368.3:n.*1573G>C
ENST00000379079.6:c.*820G>C	ENSP00000368370.2:n.*820G>C
ENST00000452863.7:c.2314G>C	ENSP00000415516.3:n.2314G>C
ENST00000530998.5:c.*820G>C	ENSP00000435307.1:n.*820G>C
NM_000378.4:c.*820G>C	NP_000369.3:n.*820G>C
NM_001198551.1:c.*820G>C , LRG_525t2:c.*820G>C	NP_001185480.1:n.*820G>C
NM_001198552.1:c.*820G>C	NP_001185481.1:n.*820G>C
NM_024424.3:c.*820G>C	NP_077742.2:n.*820G>C
NM_024426.4:c.*820G>C	NP_077744.3:n.*820G>C
NM_000378.5:c.*820G>C	NP_000369.4:n.*820G>C
NM_024424.4:c.*820G>C	NP_077742.3:n.*820G>C
NM_024426.5:c.*820G>C	NP_077744.4:n.*820G>C
NM_001367854.1:c.*820G>C	NP_001354783.1:n.*820G>C
NR_160306.1:n.2721G>C
NM_000378.6:c.*820G>C	NP_000369.4:n.*820G>C
NM_001198552.2:c.*820G>C	NP_001185481.1:n.*820G>C
NM_024424.5:c.*820G>C	NP_077742.3:n.*820G>C
NM_024426.6:c.*820G>C MANE Select	NP_077744.4:n.*820G>C