Canonical Allele Identifier: CA379960222

Gene: WT1

Linked Data

• MyVariant Identifiers: chr11:g.32421494C>G (hg19) ; chr11:g.32399948C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32399948C>G , CM000673.2:g.32399948C>G	GRCh38
NC_000011.9:g.32421494C>G , CM000673.1:g.32421494C>G	GRCh37
NC_000011.8:g.32378070C>G	NCBI36
NG_009272.1:g.40594G>C , LRG_525:g.40594G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1062G>C	ENSP00000331327.5:p.Gln354His
ENST00000379077.9:c.*297G>C	ENSP00000368368.5:n.*297G>C
ENST00000379079.8:c.462G>C	ENSP00000368370.2:p.Gln154His
ENST00000448076.9:c.1113G>C	ENSP00000413452.5:p.Gln371His
ENST00000452863.10:c.1113G>C MANE Select	ENSP00000415516.5:p.Gln371His
ENST00000526685.2:n.567G>C
ENST00000639563.3:c.1062G>C	ENSP00000492269.3:p.Gln354His
ENST00000639907.2:n.256G>C
ENST00000640146.2:c.438G>C	ENSP00000491984.2:p.Gln146His
ENST00000651459.1:c.35G>C
ENST00000651794.1:n.856G>C
ENST00000652579.1:n.273G>C
ENST00000652724.1:n.303G>C
ENST00000332351.7:c.1098G>C	ENSP00000331327.3:p.Gln366His
ENST00000379077.7:c.*297G>C	ENSP00000368368.3:n.*297G>C
ENST00000379079.6:c.462G>C	ENSP00000368370.2:p.Gln154His
ENST00000448076.7:c.1098G>C	ENSP00000413452.3:p.Gln366His
ENST00000452863.7:c.1047G>C	ENSP00000415516.3:p.Gln349His
ENST00000526685.1:c.-76G>C	ENSP00000436292.1:n.-76G>C
ENST00000527775.1:c.351G>C	ENSP00000435351.1:p.Gln117His
ENST00000527882.5:c.169G>C
ENST00000530998.5:c.411G>C	ENSP00000435307.1:p.Gln137His
NM_000378.4:c.1047G>C	NP_000369.3:p.Gln349His
NM_001198551.1:c.462G>C , LRG_525t2:c.462G>C	NP_001185480.1:p.Gln154His
NM_001198552.1:c.411G>C	NP_001185481.1:p.Gln137His
NM_024424.3:c.1098G>C	NP_077742.2:p.Gln366His
NM_024426.4:c.1098G>C	NP_077744.3:p.Gln366His
NM_000378.5:c.1062G>C	NP_000369.4:p.Gln354His
NM_024424.4:c.1113G>C	NP_077742.3:p.Gln371His
NM_024426.5:c.1113G>C	NP_077744.4:p.Gln371His
NM_001367854.1:c.-76G>C	NP_001354783.1:n.-76G>C
NR_160306.1:n.1445G>C
NM_000378.6:c.1062G>C	NP_000369.4:p.Gln354His
NM_001198552.2:c.411G>C	NP_001185481.1:p.Gln137His
NM_024424.5:c.1113G>C	NP_077742.3:p.Gln371His
NM_024426.6:c.1113G>C MANE Select	NP_077744.4:p.Gln371His