Canonical Allele Identifier: CA1962335566

Gene: WT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392769_32392771delinsCAT , CM000673.2:g.32392769_32392771delinsCAT	GRCh38
NC_000011.9:g.32414315_32414317delinsCAT , CM000673.1:g.32414315_32414317delinsCAT	GRCh37
NC_000011.8:g.32370891_32370893delinsCAT	NCBI36
NG_009272.1:g.47771_47773delinsATG , LRG_525:g.47771_47773delinsATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1214-16_1214-14delinsATG	ENSP00000331327.5:n.1214-16_1214-14delinsATG
ENST00000379077.9:c.*449-16_*449-14delinsATG	ENSP00000368368.5:n.*449-16_*449-14delinsATG
ENST00000379079.8:c.614-16_614-14delinsATG	ENSP00000368370.2:n.614-16_614-14delinsATG
ENST00000448076.9:c.1265-16_1265-14delinsATG	ENSP00000413452.5:n.1265-16_1265-14delinsATG
ENST00000452863.10:c.1265-16_1265-14delinsATG MANE Select	ENSP00000415516.5:n.1265-16_1265-14delinsATG
ENST00000526685.2:n.719-16_719-14delinsATG
ENST00000639563.3:c.1214-16_1214-14delinsATG	ENSP00000492269.3:n.1214-16_1214-14delinsATG
ENST00000639907.2:n.408-16_408-14delinsATG
ENST00000640146.2:c.590-16_590-14delinsATG	ENSP00000491984.2:n.590-16_590-14delinsATG
ENST00000650745.1:n.458_460delinsATG
ENST00000650861.1:n.1846-16_1846-14delinsATG
ENST00000651459.1:c.36-16_36-14delinsATG
ENST00000651533.1:n.295_297delinsATG
ENST00000651668.1:n.202-16_202-14delinsATG
ENST00000651794.1:n.1108-16_1108-14delinsATG
ENST00000651819.1:n.190-16_190-14delinsATG
ENST00000652579.1:n.525-16_525-14delinsATG
ENST00000652724.1:n.455-16_455-14delinsATG
ENST00000332351.7:c.1250-16_1250-14delinsATG	ENSP00000331327.3:n.1250-16_1250-14delinsATG
ENST00000379077.7:c.*449-16_*449-14delinsATG	ENSP00000368368.3:n.*449-16_*449-14delinsATG
ENST00000379079.6:c.614-16_614-14delinsATG	ENSP00000368370.2:n.614-16_614-14delinsATG
ENST00000448076.7:c.1250-16_1250-14delinsATG	ENSP00000413452.3:n.1250-16_1250-14delinsATG
ENST00000452863.7:c.1199-16_1199-14delinsATG	ENSP00000415516.3:n.1199-16_1199-14delinsATG
ENST00000527882.5:c.321-707_321-705delinsATG
ENST00000530998.5:c.563-16_563-14delinsATG	ENSP00000435307.1:n.563-16_563-14delinsATG
NM_000378.4:c.1199-16_1199-14delinsATG	NP_000369.3:n.1199-16_1199-14delinsATG
NM_001198551.1:c.614-16_614-14delinsATG , LRG_525t2:c.614-16_614-14delinsATG	NP_001185480.1:n.614-16_614-14delinsATG
NM_001198552.1:c.563-16_563-14delinsATG	NP_001185481.1:n.563-16_563-14delinsATG
NM_024424.3:c.1250-16_1250-14delinsATG	NP_077742.2:n.1250-16_1250-14delinsATG
NM_024426.4:c.1250-16_1250-14delinsATG	NP_077744.3:n.1250-16_1250-14delinsATG
NM_000378.5:c.1214-16_1214-14delinsATG	NP_000369.4:n.1214-16_1214-14delinsATG
NM_024424.4:c.1265-16_1265-14delinsATG	NP_077742.3:n.1265-16_1265-14delinsATG
NM_024426.5:c.1265-16_1265-14delinsATG	NP_077744.4:n.1265-16_1265-14delinsATG
NM_001367854.1:c.77-16_77-14delinsATG	NP_001354783.1:n.77-16_77-14delinsATG
NR_160306.1:n.1597-16_1597-14delinsATG
NM_000378.6:c.1214-16_1214-14delinsATG	NP_000369.4:n.1214-16_1214-14delinsATG
NM_001198552.2:c.563-16_563-14delinsATG	NP_001185481.1:n.563-16_563-14delinsATG
NM_024424.5:c.1265-16_1265-14delinsATG	NP_077742.3:n.1265-16_1265-14delinsATG
NM_024426.6:c.1265-16_1265-14delinsATG MANE Select	NP_077744.4:n.1265-16_1265-14delinsATG