Canonical Allele Identifier: CA379962174

Gene: WT1

Linked Data

• ClinVar Variation Id: 2934796
• ClinVar RCV Id: RCV003798498
• dbSNP Id: rs1286298624
• gnomAD v2: 11-32439178-A-G
• gnomAD v4: 11-32417632-A-G
• MyVariant Identifiers: chr11:g.32439178A>G (hg19) ; chr11:g.32417632A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32417632A>G , CM000673.2:g.32417632A>G	GRCh38
NC_000011.9:g.32439178A>G , CM000673.1:g.32439178A>G	GRCh37
NC_000011.8:g.32395754A>G	NCBI36
NG_009272.1:g.22910T>C , LRG_525:g.22910T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.910T>C	ENSP00000331327.5:p.Ser304Pro
ENST00000379077.9:c.910T>C	ENSP00000368368.5:p.Ser304Pro
ENST00000379079.8:c.259T>C	ENSP00000368370.2:p.Ser87Pro
ENST00000448076.9:c.910T>C	ENSP00000413452.5:p.Ser304Pro
ENST00000452863.10:c.910T>C MANE Select	ENSP00000415516.5:p.Ser304Pro
ENST00000639563.3:c.910T>C	ENSP00000492269.3:p.Ser304Pro
ENST00000640146.2:c.286T>C	ENSP00000491984.2:p.Ser96Pro
ENST00000332351.7:c.895T>C	ENSP00000331327.3:p.Ser299Pro
ENST00000379077.7:c.895T>C	ENSP00000368368.3:p.Ser299Pro
ENST00000379079.6:c.259T>C	ENSP00000368370.2:p.Ser87Pro
ENST00000448076.7:c.895T>C	ENSP00000413452.3:p.Ser299Pro
ENST00000452863.7:c.895T>C	ENSP00000415516.3:p.Ser299Pro
ENST00000527775.1:c.148T>C	ENSP00000435351.1:p.Ser50Pro
ENST00000530998.5:c.259T>C	ENSP00000435307.1:p.Ser87Pro
NM_000378.4:c.895T>C	NP_000369.3:p.Ser299Pro
NM_001198551.1:c.259T>C , LRG_525t2:c.259T>C	NP_001185480.1:p.Ser87Pro
NM_001198552.1:c.259T>C	NP_001185481.1:p.Ser87Pro
NM_024424.3:c.895T>C	NP_077742.2:p.Ser299Pro
NM_024426.4:c.895T>C	NP_077744.3:p.Ser299Pro
NM_000378.5:c.910T>C	NP_000369.4:p.Ser304Pro
NM_024424.4:c.910T>C	NP_077742.3:p.Ser304Pro
NM_024426.5:c.910T>C	NP_077744.4:p.Ser304Pro
NR_160306.1:n.1089T>C
NM_000378.6:c.910T>C	NP_000369.4:p.Ser304Pro
NM_001198552.2:c.259T>C	NP_001185481.1:p.Ser87Pro
NM_024424.5:c.910T>C	NP_077742.3:p.Ser304Pro
NM_024426.6:c.910T>C MANE Select	NP_077744.4:p.Ser304Pro