Canonical Allele Identifier: CA2612989398

Gene: WT1

Linked Data

• gnomAD v4: 11-32434841-T-TAGC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32434841_32434842insAGC , CM000673.2:g.32434841_32434842insAGC	GRCh38
NC_000011.9:g.32456387_32456388insAGC , CM000673.1:g.32456387_32456388insAGC	GRCh37
NC_000011.8:g.32412963_32412964insAGC	NCBI36
NG_009272.1:g.5700_5701insGCT , LRG_525:g.5700_5701insGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.519_520insGCT	ENSP00000331327.5:p.Phe173_Thr174insAla
ENST00000379077.9:c.519_520insGCT	ENSP00000368368.5:p.Phe173_Thr174insAla
ENST00000448076.9:c.519_520insGCT	ENSP00000413452.5:p.Phe173_Thr174insAla
ENST00000452863.10:c.519_520insGCT MANE Select	ENSP00000415516.5:p.Phe173_Thr174insAla
ENST00000639563.3:c.519_520insGCT	ENSP00000492269.3:p.Phe173_Thr174insAla
ENST00000332351.7:c.504_505insGCT	ENSP00000331327.3:p.Phe168_Thr169insAla
ENST00000379077.7:c.504_505insGCT	ENSP00000368368.3:p.Phe168_Thr169insAla
ENST00000448076.7:c.504_505insGCT	ENSP00000413452.3:p.Phe168_Thr169insAla
ENST00000452863.7:c.504_505insGCT	ENSP00000415516.3:p.Phe168_Thr169insAla
NM_000378.4:c.504_505insGCT	NP_000369.3:p.Phe168_Thr169insAla
NM_024424.3:c.504_505insGCT	NP_077742.2:p.Phe168_Thr169insAla
NM_024426.4:c.504_505insGCT	NP_077744.3:p.Phe168_Thr169insAla
NM_000378.5:c.519_520insGCT	NP_000369.4:p.Phe173_Thr174insAla
NM_024424.4:c.519_520insGCT	NP_077742.3:p.Phe173_Thr174insAla
NM_024426.5:c.519_520insGCT	NP_077744.4:p.Phe173_Thr174insAla
NR_160306.1:n.698_699insGCT
NM_000378.6:c.519_520insGCT	NP_000369.4:p.Phe173_Thr174insAla
NM_024424.5:c.519_520insGCT	NP_077742.3:p.Phe173_Thr174insAla
NM_024426.6:c.519_520insGCT MANE Select	NP_077744.4:p.Phe173_Thr174insAla