Canonical Allele Identifier: CA2612986608

Gene: WT1

Linked Data

• gnomAD v4: 11-32400183-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32400183G>A , CM000673.2:g.32400183G>A	GRCh38
NC_000011.9:g.32421729G>A , CM000673.1:g.32421729G>A	GRCh37
NC_000011.8:g.32378305G>A	NCBI36
NG_009272.1:g.40359C>T , LRG_525:g.40359C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.966-139C>T	ENSP00000331327.5:n.966-139C>T
ENST00000379077.9:c.*201-139C>T	ENSP00000368368.5:n.*201-139C>T
ENST00000379079.8:c.366-139C>T	ENSP00000368370.2:n.366-139C>T
ENST00000448076.9:c.1017-139C>T	ENSP00000413452.5:n.1017-139C>T
ENST00000452863.10:c.1017-139C>T MANE Select	ENSP00000415516.5:n.1017-139C>T
ENST00000526685.2:n.433C>T
ENST00000639563.3:c.966-139C>T	ENSP00000492269.3:n.966-139C>T
ENST00000639907.2:n.21C>T
ENST00000640146.2:c.342-139C>T	ENSP00000491984.2:n.342-139C>T
ENST00000651794.1:n.760-139C>T
ENST00000652579.1:n.177-139C>T
ENST00000652724.1:n.169C>T
ENST00000332351.7:c.1002-139C>T	ENSP00000331327.3:n.1002-139C>T
ENST00000379077.7:c.*201-139C>T	ENSP00000368368.3:n.*201-139C>T
ENST00000379079.6:c.366-139C>T	ENSP00000368370.2:n.366-139C>T
ENST00000448076.7:c.1002-139C>T	ENSP00000413452.3:n.1002-139C>T
ENST00000452863.7:c.951-139C>T	ENSP00000415516.3:n.951-139C>T
ENST00000526685.1:c.-210C>T	ENSP00000436292.1:n.-210C>T
ENST00000527775.1:c.255-139C>T	ENSP00000435351.1:n.255-139C>T
ENST00000527882.5:c.73-139C>T
ENST00000530998.5:c.315-139C>T	ENSP00000435307.1:n.315-139C>T
NM_000378.4:c.951-139C>T	NP_000369.3:n.951-139C>T
NM_001198551.1:c.366-139C>T , LRG_525t2:c.366-139C>T	NP_001185480.1:n.366-139C>T
NM_001198552.1:c.315-139C>T	NP_001185481.1:n.315-139C>T
NM_024424.3:c.1002-139C>T	NP_077742.2:n.1002-139C>T
NM_024426.4:c.1002-139C>T	NP_077744.3:n.1002-139C>T
NM_000378.5:c.966-139C>T	NP_000369.4:n.966-139C>T
NM_024424.4:c.1017-139C>T	NP_077742.3:n.1017-139C>T
NM_024426.5:c.1017-139C>T	NP_077744.4:n.1017-139C>T
NM_001367854.1:c.-210C>T	NP_001354783.1:n.-210C>T
NR_160306.1:n.1349-139C>T
NM_000378.6:c.966-139C>T	NP_000369.4:n.966-139C>T
NM_001198552.2:c.315-139C>T	NP_001185481.1:n.315-139C>T
NM_024424.5:c.1017-139C>T	NP_077742.3:n.1017-139C>T
NM_024426.6:c.1017-139C>T MANE Select	NP_077744.4:n.1017-139C>T