Canonical Allele Identifier: CA2612986659

Gene: WT1

Linked Data

• gnomAD v4: 11-32400232-C-CCT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32400233_32400234insTC , CM000673.2:g.32400233_32400234insTC	GRCh38
NC_000011.9:g.32421779_32421780insTC , CM000673.1:g.32421779_32421780insTC	GRCh37
NC_000011.8:g.32378355_32378356insTC	NCBI36
NG_009272.1:g.40309_40310insAG , LRG_525:g.40309_40310insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.966-189_966-188insAG	ENSP00000331327.5:n.966-189_966-188insAG
ENST00000379077.9:c.*201-189_*201-188insAG	ENSP00000368368.5:n.*201-189_*201-188insAG
ENST00000379079.8:c.366-189_366-188insAG	ENSP00000368370.2:n.366-189_366-188insAG
ENST00000448076.9:c.1017-189_1017-188insAG	ENSP00000413452.5:n.1017-189_1017-188insAG
ENST00000452863.10:c.1017-189_1017-188insAG MANE Select	ENSP00000415516.5:n.1017-189_1017-188insAG
ENST00000526685.2:n.383_384insAG
ENST00000639563.3:c.966-189_966-188insAG	ENSP00000492269.3:n.966-189_966-188insAG
ENST00000640146.2:c.342-189_342-188insAG	ENSP00000491984.2:n.342-189_342-188insAG
ENST00000651794.1:n.760-189_760-188insAG
ENST00000652579.1:n.177-189_177-188insAG
ENST00000652724.1:n.119_120insAG
ENST00000332351.7:c.1002-189_1002-188insAG	ENSP00000331327.3:n.1002-189_1002-188insAG
ENST00000379077.7:c.*201-189_*201-188insAG	ENSP00000368368.3:n.*201-189_*201-188insAG
ENST00000379079.6:c.366-189_366-188insAG	ENSP00000368370.2:n.366-189_366-188insAG
ENST00000448076.7:c.1002-189_1002-188insAG	ENSP00000413452.3:n.1002-189_1002-188insAG
ENST00000452863.7:c.951-189_951-188insAG	ENSP00000415516.3:n.951-189_951-188insAG
ENST00000526685.1:c.-260_-259insAG	ENSP00000436292.1:n.-260_-259insAG
ENST00000527775.1:c.255-189_255-188insAG	ENSP00000435351.1:n.255-189_255-188insAG
ENST00000527882.5:c.73-189_73-188insAG
ENST00000530998.5:c.315-189_315-188insAG	ENSP00000435307.1:n.315-189_315-188insAG
NM_000378.4:c.951-189_951-188insAG	NP_000369.3:n.951-189_951-188insAG
NM_001198551.1:c.366-189_366-188insAG , LRG_525t2:c.366-189_366-188insAG	NP_001185480.1:n.366-189_366-188insAG
NM_001198552.1:c.315-189_315-188insAG	NP_001185481.1:n.315-189_315-188insAG
NM_024424.3:c.1002-189_1002-188insAG	NP_077742.2:n.1002-189_1002-188insAG
NM_024426.4:c.1002-189_1002-188insAG	NP_077744.3:n.1002-189_1002-188insAG
NM_000378.5:c.966-189_966-188insAG	NP_000369.4:n.966-189_966-188insAG
NM_024424.4:c.1017-189_1017-188insAG	NP_077742.3:n.1017-189_1017-188insAG
NM_024426.5:c.1017-189_1017-188insAG	NP_077744.4:n.1017-189_1017-188insAG
NM_001367854.1:c.-260_-259insAG	NP_001354783.1:n.-260_-259insAG
NR_160306.1:n.1349-189_1349-188insAG
NM_000378.6:c.966-189_966-188insAG	NP_000369.4:n.966-189_966-188insAG
NM_001198552.2:c.315-189_315-188insAG	NP_001185481.1:n.315-189_315-188insAG
NM_024424.5:c.1017-189_1017-188insAG	NP_077742.3:n.1017-189_1017-188insAG
NM_024426.6:c.1017-189_1017-188insAG MANE Select	NP_077744.4:n.1017-189_1017-188insAG