Canonical Allele Identifier: CA064811

Gene: WT1

Linked Data

• ClinVar Variation Id: 241480
• ClinVar RCV Id: RCV000329886 ; RCV000276013 ; RCV000389047 ; RCV000832485 ; RCV001083587 ; RCV002257599
• dbSNP Id: rs547333427
• ExAC: 11:32456598 G / T
• gnomAD v2: 11-32456598-G-T
• gnomAD v3: 11-32435052-G-T
• gnomAD v4: 11-32435052-G-T
• MyVariant Identifiers: chr11:g.32456598G>T (hg19) ; chr11:g.32435052G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32435052G>T , CM000673.2:g.32435052G>T	GRCh38
NC_000011.9:g.32456598G>T , CM000673.1:g.32456598G>T	GRCh37
NC_000011.8:g.32413174G>T	NCBI36
NG_009272.1:g.5490C>A , LRG_525:g.5490C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.309C>A	ENSP00000331327.5:p.Gly103=
ENST00000379077.9:c.309C>A	ENSP00000368368.5:p.Gly103=
ENST00000448076.9:c.309C>A	ENSP00000413452.5:p.Gly103=
ENST00000452863.10:c.309C>A MANE Select	ENSP00000415516.5:p.Gly103=
ENST00000639563.3:c.309C>A	ENSP00000492269.3:p.Gly103=
ENST00000332351.7:c.294C>A	ENSP00000331327.3:p.Gly98=
ENST00000379077.7:c.294C>A	ENSP00000368368.3:p.Gly98=
ENST00000448076.7:c.294C>A	ENSP00000413452.3:p.Gly98=
ENST00000452863.7:c.294C>A	ENSP00000415516.3:p.Gly98=
NM_000378.4:c.294C>A	NP_000369.3:p.Gly98=
NM_024424.3:c.294C>A	NP_077742.2:p.Gly98=
NM_024426.4:c.294C>A	NP_077744.3:p.Gly98=
NM_000378.5:c.309C>A	NP_000369.4:p.Gly103=
NM_024424.4:c.309C>A	NP_077742.3:p.Gly103=
NM_024426.5:c.309C>A	NP_077744.4:p.Gly103=
NR_160306.1:n.488C>A
NM_000378.6:c.309C>A	NP_000369.4:p.Gly103=
NM_024424.5:c.309C>A	NP_077742.3:p.Gly103=
NM_024426.6:c.309C>A MANE Select	NP_077744.4:p.Gly103=