Canonical Allele Identifier: CA2612989401

Gene: WT1

Linked Data

• gnomAD v4: 11-32434846-T-TCC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32434846_32434847insCC , CM000673.2:g.32434846_32434847insCC	GRCh38
NC_000011.9:g.32456392_32456393insCC , CM000673.1:g.32456392_32456393insCC	GRCh37
NC_000011.8:g.32412968_32412969insCC	NCBI36
NG_009272.1:g.5695_5696insGG , LRG_525:g.5695_5696insGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.514_515insGG	ENSP00000331327.5:p.Gln172ArgfsTer?
ENST00000379077.9:c.514_515insGG	ENSP00000368368.5:p.Gln172ArgfsTer?
ENST00000448076.9:c.514_515insGG	ENSP00000413452.5:p.Gln172ArgfsTer?
ENST00000452863.10:c.514_515insGG MANE Select	ENSP00000415516.5:p.Gln172ArgfsTer?
ENST00000639563.3:c.514_515insGG	ENSP00000492269.3:p.Gln172ArgfsTer?
ENST00000332351.7:c.499_500insGG	ENSP00000331327.3:p.Gln167ArgfsTer?
ENST00000379077.7:c.499_500insGG	ENSP00000368368.3:p.Gln167ArgfsTer?
ENST00000448076.7:c.499_500insGG	ENSP00000413452.3:p.Gln167ArgfsTer?
ENST00000452863.7:c.499_500insGG	ENSP00000415516.3:p.Gln167ArgfsTer?
NM_000378.4:c.499_500insGG	NP_000369.3:p.Gln167ArgfsTer?
NM_024424.3:c.499_500insGG	NP_077742.2:p.Gln167ArgfsTer?
NM_024426.4:c.499_500insGG	NP_077744.3:p.Gln167ArgfsTer?
NM_000378.5:c.514_515insGG	NP_000369.4:p.Gln172ArgfsTer?
NM_024424.4:c.514_515insGG	NP_077742.3:p.Gln172ArgfsTer?
NM_024426.5:c.514_515insGG	NP_077744.4:p.Gln172ArgfsTer?
NR_160306.1:n.693_694insGG
NM_000378.6:c.514_515insGG	NP_000369.4:p.Gln172ArgfsTer?
NM_024424.5:c.514_515insGG	NP_077742.3:p.Gln172ArgfsTer?
NM_024426.6:c.514_515insGG MANE Select	NP_077744.4:p.Gln172ArgfsTer?