Canonical Allele Identifier: CA1962340428

Gene: WT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32399974T= , CM000673.2:g.32399974T=	GRCh38
NC_000011.9:g.32421520T= , CM000673.1:g.32421520T=	GRCh37
NC_000011.8:g.32378096T=	NCBI36
NG_009272.1:g.40568A= , LRG_525:g.40568A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1036A=	ENSP00000331327.5:p.Thr346=
ENST00000379077.9:c.*271A=	ENSP00000368368.5:n.*271A=
ENST00000379079.8:c.436A=	ENSP00000368370.2:p.Thr146=
ENST00000448076.9:c.1087A=	ENSP00000413452.5:p.Thr363=
ENST00000452863.10:c.1087A= MANE Select	ENSP00000415516.5:p.Thr363=
ENST00000526685.2:n.541A=
ENST00000639563.3:c.1036A=	ENSP00000492269.3:p.Thr346=
ENST00000639907.2:n.230A=
ENST00000640146.2:c.412A=	ENSP00000491984.2:p.Thr138=
ENST00000651459.1:c.9A=
ENST00000651794.1:n.830A=
ENST00000652579.1:n.247A=
ENST00000652724.1:n.277A=
ENST00000332351.7:c.1072A=	ENSP00000331327.3:p.Thr358=
ENST00000379077.7:c.*271A=	ENSP00000368368.3:n.*271A=
ENST00000379079.6:c.436A=	ENSP00000368370.2:p.Thr146=
ENST00000448076.7:c.1072A=	ENSP00000413452.3:p.Thr358=
ENST00000452863.7:c.1021A=	ENSP00000415516.3:p.Thr341=
ENST00000526685.1:c.-102A=	ENSP00000436292.1:n.-102A=
ENST00000527775.1:c.325A=	ENSP00000435351.1:p.Thr109=
ENST00000527882.5:c.143A=
ENST00000530998.5:c.385A=	ENSP00000435307.1:p.Thr129=
NM_000378.4:c.1021A=	NP_000369.3:p.Thr341=
NM_001198551.1:c.436A= , LRG_525t2:c.436A=	NP_001185480.1:p.Thr146=
NM_001198552.1:c.385A=	NP_001185481.1:p.Thr129=
NM_024424.3:c.1072A=	NP_077742.2:p.Thr358=
NM_024426.4:c.1072A=	NP_077744.3:p.Thr358=
NM_000378.5:c.1036A=	NP_000369.4:p.Thr346=
NM_024424.4:c.1087A=	NP_077742.3:p.Thr363=
NM_024426.5:c.1087A=	NP_077744.4:p.Thr363=
NM_001367854.1:c.-102A=	NP_001354783.1:n.-102A=
NR_160306.1:n.1419A=
NM_000378.6:c.1036A=	NP_000369.4:p.Thr346=
NM_001198552.2:c.385A=	NP_001185481.1:p.Thr129=
NM_024424.5:c.1087A=	NP_077742.3:p.Thr363=
NM_024426.6:c.1087A= MANE Select	NP_077744.4:p.Thr363=