Canonical Allele Identifier: CA379966185

Gene: WT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32435165C>T , CM000673.2:g.32435165C>T	GRCh38
NC_000011.9:g.32456711C>T , CM000673.1:g.32456711C>T	GRCh37
NC_000011.8:g.32413287C>T	NCBI36
NG_009272.1:g.5377G>A , LRG_525:g.5377G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_024426.6:c.196G>A MANE Select	NP_077744.4:p.Ala66Thr
ENST00000452863.10:c.196G>A MANE Select	ENSP00000415516.5:p.Ala66Thr
NM_000378.4:c.181G>A	NP_000369.3:p.Ala61Thr
NM_000378.5:c.196G>A	NP_000369.4:p.Ala66Thr
NM_000378.6:c.196G>A	NP_000369.4:p.Ala66Thr
NM_024424.3:c.181G>A	NP_077742.2:p.Ala61Thr
NM_024424.4:c.196G>A	NP_077742.3:p.Ala66Thr
NM_024424.5:c.196G>A	NP_077742.3:p.Ala66Thr
NM_024426.4:c.181G>A	NP_077744.3:p.Ala61Thr
NM_024426.5:c.196G>A	NP_077744.4:p.Ala66Thr
NR_160306.1:n.375G>A
ENST00000332351.7:c.181G>A	ENSP00000331327.3:p.Ala61Thr
ENST00000332351.9:c.196G>A	ENSP00000331327.5:p.Ala66Thr
ENST00000379077.7:c.181G>A	ENSP00000368368.3:p.Ala61Thr
ENST00000379077.9:c.196G>A	ENSP00000368368.5:p.Ala66Thr
ENST00000448076.7:c.181G>A	ENSP00000413452.3:p.Ala61Thr
ENST00000448076.9:c.196G>A	ENSP00000413452.5:p.Ala66Thr
ENST00000452863.7:c.181G>A	ENSP00000415516.3:p.Ala61Thr
ENST00000639563.3:c.196G>A	ENSP00000492269.3:p.Ala66Thr