Canonical Allele Identifier: CA10638312

Gene: WT1

Linked Data

• ClinVar Variation Id: 304371
• ClinVar RCV Id: RCV000288713 ; RCV000345969 ; RCV000380791
• dbSNP Id: rs886048210
• MyVariant Identifiers: chr11:g.32409379A>G (hg19) ; chr11:g.32387833A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32387833A>G , CM000673.2:g.32387833A>G	GRCh38
NC_000011.9:g.32409379A>G , CM000673.1:g.32409379A>G	GRCh37
NC_000011.8:g.32365955A>G	NCBI36
NG_009272.1:g.52709T>C , LRG_525:g.52709T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.*1225T>C	ENSP00000331327.5:n.*1225T>C
ENST00000379077.9:c.*1978T>C	ENSP00000368368.5:n.*1978T>C
ENST00000379079.8:c.*1225T>C	ENSP00000368370.2:n.*1225T>C
ENST00000452863.10:c.*1225T>C MANE Select	ENSP00000415516.5:n.*1225T>C
ENST00000332351.7:c.*1225T>C	ENSP00000331327.3:n.*1225T>C
ENST00000379077.7:c.*1978T>C	ENSP00000368368.3:n.*1978T>C
ENST00000379079.6:c.*1225T>C	ENSP00000368370.2:n.*1225T>C
ENST00000452863.7:c.2719T>C	ENSP00000415516.3:n.2719T>C
ENST00000530998.5:c.*1225T>C	ENSP00000435307.1:n.*1225T>C
NM_000378.4:c.*1225T>C	NP_000369.3:n.*1225T>C
NM_001198551.1:c.*1225T>C , LRG_525t2:c.*1225T>C	NP_001185480.1:n.*1225T>C
NM_001198552.1:c.*1225T>C	NP_001185481.1:n.*1225T>C
NM_024424.3:c.*1225T>C	NP_077742.2:n.*1225T>C
NM_024426.4:c.*1225T>C	NP_077744.3:n.*1225T>C
NM_000378.5:c.*1225T>C	NP_000369.4:n.*1225T>C
NM_024424.4:c.*1225T>C	NP_077742.3:n.*1225T>C
NM_024426.5:c.*1225T>C	NP_077744.4:n.*1225T>C
NM_001367854.1:c.*1225T>C	NP_001354783.1:n.*1225T>C
NR_160306.1:n.3126T>C
NM_000378.6:c.*1225T>C	NP_000369.4:n.*1225T>C
NM_001198552.2:c.*1225T>C	NP_001185481.1:n.*1225T>C
NM_024424.5:c.*1225T>C	NP_077742.3:n.*1225T>C
NM_024426.6:c.*1225T>C MANE Select	NP_077744.4:n.*1225T>C