Canonical Allele Identifier: CA2612970541

Gene: WT1

Linked Data

• gnomAD v4: 11-32387961-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32387961G>T , CM000673.2:g.32387961G>T	GRCh38
NC_000011.9:g.32409507G>T , CM000673.1:g.32409507G>T	GRCh37
NC_000011.8:g.32366083G>T	NCBI36
NG_009272.1:g.52581C>A , LRG_525:g.52581C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.*1097C>A	ENSP00000331327.5:n.*1097C>A
ENST00000379077.9:c.*1850C>A	ENSP00000368368.5:n.*1850C>A
ENST00000379079.8:c.*1097C>A	ENSP00000368370.2:n.*1097C>A
ENST00000452863.10:c.*1097C>A MANE Select	ENSP00000415516.5:n.*1097C>A
ENST00000651819.1:n.1591C>A
ENST00000332351.7:c.*1097C>A	ENSP00000331327.3:n.*1097C>A
ENST00000379077.7:c.*1850C>A	ENSP00000368368.3:n.*1850C>A
ENST00000379079.6:c.*1097C>A	ENSP00000368370.2:n.*1097C>A
ENST00000452863.7:c.2591C>A	ENSP00000415516.3:n.2591C>A
ENST00000530998.5:c.*1097C>A	ENSP00000435307.1:n.*1097C>A
NM_000378.4:c.*1097C>A	NP_000369.3:n.*1097C>A
NM_001198551.1:c.*1097C>A , LRG_525t2:c.*1097C>A	NP_001185480.1:n.*1097C>A
NM_001198552.1:c.*1097C>A	NP_001185481.1:n.*1097C>A
NM_024424.3:c.*1097C>A	NP_077742.2:n.*1097C>A
NM_024426.4:c.*1097C>A	NP_077744.3:n.*1097C>A
NM_000378.5:c.*1097C>A	NP_000369.4:n.*1097C>A
NM_024424.4:c.*1097C>A	NP_077742.3:n.*1097C>A
NM_024426.5:c.*1097C>A	NP_077744.4:n.*1097C>A
NM_001367854.1:c.*1097C>A	NP_001354783.1:n.*1097C>A
NR_160306.1:n.2998C>A
NM_000378.6:c.*1097C>A	NP_000369.4:n.*1097C>A
NM_001198552.2:c.*1097C>A	NP_001185481.1:n.*1097C>A
NM_024424.5:c.*1097C>A	NP_077742.3:n.*1097C>A
NM_024426.6:c.*1097C>A MANE Select	NP_077744.4:n.*1097C>A