Canonical Allele Identifier: CA1962335271

Gene: WT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392020_32392023delinsGGGA , CM000673.2:g.32392020_32392023delinsGGGA	GRCh38
NC_000011.9:g.32413566_32413569delinsGGGA , CM000673.1:g.32413566_32413569delinsGGGA	GRCh37
NC_000011.8:g.32370142_32370145delinsGGGA	NCBI36
NG_009272.1:g.48519_48522delinsTCCC , LRG_525:g.48519_48522delinsTCCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1345_1348delinsTCCC	ENSP00000331327.5:p.Ser449=
ENST00000379077.9:c.*580_*583delinsTCCC	ENSP00000368368.5:n.*580_*583delinsTCCC
ENST00000379079.8:c.745_748delinsTCCC	ENSP00000368370.2:p.Ser249=
ENST00000448076.9:c.1396_1399delinsTCCC	ENSP00000413452.5:p.Ser466=
ENST00000452863.10:c.1396_1399delinsTCCC MANE Select	ENSP00000415516.5:p.Ser466=
ENST00000526685.2:n.850_853delinsTCCC
ENST00000639563.3:c.1345_1348delinsTCCC	ENSP00000492269.3:p.Ser449=
ENST00000639907.2:n.539_542delinsTCCC
ENST00000640146.2:c.721_724delinsTCCC	ENSP00000491984.2:p.Ser241=
ENST00000650745.1:n.1206_1209delinsTCCC
ENST00000650861.1:n.1977_1980delinsTCCC
ENST00000650986.1:n.59_62delinsTCCC
ENST00000651459.1:c.167_170delinsTCCC
ENST00000651533.1:n.442_445delinsTCCC
ENST00000651668.1:n.333_336delinsTCCC
ENST00000651794.1:n.1239_1242delinsTCCC
ENST00000651819.1:n.321_324delinsTCCC
ENST00000652579.1:n.656_659delinsTCCC
ENST00000652724.1:n.586_589delinsTCCC
ENST00000332351.7:c.1381_1384delinsTCCC	ENSP00000331327.3:p.Ser461=
ENST00000379077.7:c.*580_*583delinsTCCC	ENSP00000368368.3:n.*580_*583delinsTCCC
ENST00000379079.6:c.745_748delinsTCCC	ENSP00000368370.2:p.Ser249=
ENST00000448076.7:c.1381_1384delinsTCCC	ENSP00000413452.3:p.Ser461=
ENST00000452863.7:c.1330_1333delinsTCCC	ENSP00000415516.3:p.Ser444=
ENST00000527882.5:c.362_365delinsTCCC
ENST00000530998.5:c.694_697delinsTCCC	ENSP00000435307.1:p.Ser232=
NM_000378.4:c.1330_1333delinsTCCC	NP_000369.3:p.Ser444=
NM_001198551.1:c.745_748delinsTCCC , LRG_525t2:c.745_748delinsTCCC	NP_001185480.1:p.Ser249=
NM_001198552.1:c.694_697delinsTCCC	NP_001185481.1:p.Ser232=
NM_024424.3:c.1381_1384delinsTCCC	NP_077742.2:p.Ser461=
NM_024426.4:c.1381_1384delinsTCCC	NP_077744.3:p.Ser461=
NM_000378.5:c.1345_1348delinsTCCC	NP_000369.4:p.Ser449=
NM_024424.4:c.1396_1399delinsTCCC	NP_077742.3:p.Ser466=
NM_024426.5:c.1396_1399delinsTCCC	NP_077744.4:p.Ser466=
NM_001367854.1:c.208_211delinsTCCC	NP_001354783.1:p.Ser70=
NR_160306.1:n.1728_1731delinsTCCC
NM_000378.6:c.1345_1348delinsTCCC	NP_000369.4:p.Ser449=
NM_001198552.2:c.694_697delinsTCCC	NP_001185481.1:p.Ser232=
NM_024424.5:c.1396_1399delinsTCCC	NP_077742.3:p.Ser466=
NM_024426.6:c.1396_1399delinsTCCC MANE Select	NP_077744.4:p.Ser466=