Canonical Allele Identifier: CA379959860

Gene: WT1

Linked Data

• MyVariant Identifiers: chr11:g.32417845A>G (hg19) ; chr11:g.32396299A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32396299A>G , CM000673.2:g.32396299A>G	GRCh38
NC_000011.9:g.32417845A>G , CM000673.1:g.32417845A>G	GRCh37
NC_000011.8:g.32374421A>G	NCBI36
NG_009272.1:g.44243T>C , LRG_525:g.44243T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1171T>C	ENSP00000331327.5:p.Phe391Leu
ENST00000379077.9:c.*406T>C	ENSP00000368368.5:n.*406T>C
ENST00000379079.8:c.571T>C	ENSP00000368370.2:p.Phe191Leu
ENST00000448076.9:c.1222T>C	ENSP00000413452.5:p.Phe408Leu
ENST00000452863.10:c.1222T>C MANE Select	ENSP00000415516.5:p.Phe408Leu
ENST00000526685.2:n.676T>C
ENST00000639563.3:c.1171T>C	ENSP00000492269.3:p.Phe391Leu
ENST00000639907.2:n.365T>C
ENST00000640146.2:c.547T>C	ENSP00000491984.2:p.Phe183Leu
ENST00000650861.1:n.1803T>C
ENST00000651459.1:c.36-3544T>C
ENST00000651668.1:n.159T>C
ENST00000651794.1:n.965T>C
ENST00000651819.1:n.147T>C
ENST00000652579.1:n.382T>C
ENST00000652724.1:n.412T>C
ENST00000332351.7:c.1207T>C	ENSP00000331327.3:p.Phe403Leu
ENST00000379077.7:c.*406T>C	ENSP00000368368.3:n.*406T>C
ENST00000379079.6:c.571T>C	ENSP00000368370.2:p.Phe191Leu
ENST00000448076.7:c.1207T>C	ENSP00000413452.3:p.Phe403Leu
ENST00000452863.7:c.1156T>C	ENSP00000415516.3:p.Phe386Leu
ENST00000526685.1:c.34T>C	ENSP00000436292.1:p.Phe12Leu
ENST00000527882.5:c.278T>C
ENST00000530998.5:c.520T>C	ENSP00000435307.1:p.Phe174Leu
NM_000378.4:c.1156T>C	NP_000369.3:p.Phe386Leu
NM_001198551.1:c.571T>C , LRG_525t2:c.571T>C	NP_001185480.1:p.Phe191Leu
NM_001198552.1:c.520T>C	NP_001185481.1:p.Phe174Leu
NM_024424.3:c.1207T>C	NP_077742.2:p.Phe403Leu
NM_024426.4:c.1207T>C	NP_077744.3:p.Phe403Leu
NM_000378.5:c.1171T>C	NP_000369.4:p.Phe391Leu
NM_024424.4:c.1222T>C	NP_077742.3:p.Phe408Leu
NM_024426.5:c.1222T>C	NP_077744.4:p.Phe408Leu
NM_001367854.1:c.34T>C	NP_001354783.1:p.Phe12Leu
NR_160306.1:n.1554T>C
NM_000378.6:c.1171T>C	NP_000369.4:p.Phe391Leu
NM_001198552.2:c.520T>C	NP_001185481.1:p.Phe174Leu
NM_024424.5:c.1222T>C	NP_077742.3:p.Phe408Leu
NM_024426.6:c.1222T>C MANE Select	NP_077744.4:p.Phe408Leu