Canonical Allele Identifier: CA064961

Gene: WT1

Linked Data

• ClinVar Variation Id: 1095994
• ClinVar RCV Id: RCV001417092 ; RCV004006942
• dbSNP Id: rs753238865
• ExAC: 11:32456436 G / A
• gnomAD v2: 11-32456436-G-A
• gnomAD v4: 11-32434890-G-A
• COSMIC: COSM5637025 ; COSM5637026
• MyVariant Identifiers: chr11:g.32456436G>A (hg19) ; chr11:g.32434890G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32434890G>A , CM000673.2:g.32434890G>A	GRCh38
NC_000011.9:g.32456436G>A , CM000673.1:g.32456436G>A	GRCh37
NC_000011.8:g.32413012G>A	NCBI36
NG_009272.1:g.5652C>T , LRG_525:g.5652C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.471C>T	ENSP00000331327.5:p.His157=
ENST00000379077.9:c.471C>T	ENSP00000368368.5:p.His157=
ENST00000448076.9:c.471C>T	ENSP00000413452.5:p.His157=
ENST00000452863.10:c.471C>T MANE Select	ENSP00000415516.5:p.His157=
ENST00000639563.3:c.471C>T	ENSP00000492269.3:p.His157=
ENST00000332351.7:c.456C>T	ENSP00000331327.3:p.His152=
ENST00000379077.7:c.456C>T	ENSP00000368368.3:p.His152=
ENST00000448076.7:c.456C>T	ENSP00000413452.3:p.His152=
ENST00000452863.7:c.456C>T	ENSP00000415516.3:p.His152=
NM_000378.4:c.456C>T	NP_000369.3:p.His152=
NM_024424.3:c.456C>T	NP_077742.2:p.His152=
NM_024426.4:c.456C>T	NP_077744.3:p.His152=
NM_000378.5:c.471C>T	NP_000369.4:p.His157=
NM_024424.4:c.471C>T	NP_077742.3:p.His157=
NM_024426.5:c.471C>T	NP_077744.4:p.His157=
NR_160306.1:n.650C>T
NM_000378.6:c.471C>T	NP_000369.4:p.His157=
NM_024424.5:c.471C>T	NP_077742.3:p.His157=
NM_024426.6:c.471C>T MANE Select	NP_077744.4:p.His157=