Canonical Allele Identifier: CA473565304

Gene: WT1

Linked Data

• ClinVar Variation Id: 543146
• ClinVar RCV Id: RCV000653809
• dbSNP Id: rs1554939066
• MyVariant Identifiers: chr11:g.32413543G>A (hg19) ; chr11:g.32391997G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32391997G>A , CM000673.2:g.32391997G>A	GRCh38
NC_000011.9:g.32413543G>A , CM000673.1:g.32413543G>A	GRCh37
NC_000011.8:g.32370119G>A	NCBI36
NG_009272.1:g.48545C>T , LRG_525:g.48545C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1371C>T	ENSP00000331327.5:p.His457=
ENST00000379077.9:c.*606C>T	ENSP00000368368.5:n.*606C>T
ENST00000379079.8:c.771C>T	ENSP00000368370.2:p.His257=
ENST00000448076.9:c.1422C>T	ENSP00000413452.5:p.His474=
ENST00000452863.10:c.1422C>T MANE Select	ENSP00000415516.5:p.His474=
ENST00000526685.2:n.876C>T
ENST00000639563.3:c.1371C>T	ENSP00000492269.3:p.His457=
ENST00000639907.2:n.565C>T
ENST00000640146.2:c.747C>T	ENSP00000491984.2:p.His249=
ENST00000650745.1:n.1232C>T
ENST00000650861.1:n.2003C>T
ENST00000650986.1:n.85C>T
ENST00000651459.1:c.193C>T
ENST00000651533.1:n.468C>T
ENST00000651668.1:n.359C>T
ENST00000651794.1:n.1265C>T
ENST00000651819.1:n.347C>T
ENST00000652579.1:n.682C>T
ENST00000652724.1:n.612C>T
ENST00000332351.7:c.1407C>T	ENSP00000331327.3:p.His469=
ENST00000379077.7:c.*606C>T	ENSP00000368368.3:n.*606C>T
ENST00000379079.6:c.771C>T	ENSP00000368370.2:p.His257=
ENST00000448076.7:c.1407C>T	ENSP00000413452.3:p.His469=
ENST00000452863.7:c.1356C>T	ENSP00000415516.3:p.His452=
ENST00000527882.5:c.388C>T
ENST00000530998.5:c.720C>T	ENSP00000435307.1:p.His240=
NM_000378.4:c.1356C>T	NP_000369.3:p.His452=
NM_001198551.1:c.771C>T , LRG_525t2:c.771C>T	NP_001185480.1:p.His257=
NM_001198552.1:c.720C>T	NP_001185481.1:p.His240=
NM_024424.3:c.1407C>T	NP_077742.2:p.His469=
NM_024426.4:c.1407C>T	NP_077744.3:p.His469=
NM_000378.5:c.1371C>T	NP_000369.4:p.His457=
NM_024424.4:c.1422C>T	NP_077742.3:p.His474=
NM_024426.5:c.1422C>T	NP_077744.4:p.His474=
NM_001367854.1:c.234C>T	NP_001354783.1:p.His78=
NR_160306.1:n.1754C>T
NM_000378.6:c.1371C>T	NP_000369.4:p.His457=
NM_001198552.2:c.720C>T	NP_001185481.1:p.His240=
NM_024424.5:c.1422C>T	NP_077742.3:p.His474=
NM_024426.6:c.1422C>T MANE Select	NP_077744.4:p.His474=