Canonical Allele Identifier: CA1962318463

Gene: WT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32417644_32417645delinsAT , CM000673.2:g.32417644_32417645delinsAT	GRCh38
NC_000011.9:g.32439190_32439191delinsAT , CM000673.1:g.32439190_32439191delinsAT	GRCh37
NC_000011.8:g.32395766_32395767delinsAT	NCBI36
NG_009272.1:g.22897_22898delinsAT , LRG_525:g.22897_22898delinsAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.897_898delinsAT	ENSP00000331327.5:p.Leu299=
ENST00000379077.9:c.897_898delinsAT	ENSP00000368368.5:p.Leu299=
ENST00000379079.8:c.246_247delinsAT	ENSP00000368370.2:p.Leu82=
ENST00000448076.9:c.897_898delinsAT	ENSP00000413452.5:p.Leu299=
ENST00000452863.10:c.897_898delinsAT MANE Select	ENSP00000415516.5:p.Leu299=
ENST00000639563.3:c.897_898delinsAT	ENSP00000492269.3:p.Leu299=
ENST00000640146.2:c.273_274delinsAT	ENSP00000491984.2:p.Leu91=
ENST00000332351.7:c.882_883delinsAT	ENSP00000331327.3:p.Leu294=
ENST00000379077.7:c.882_883delinsAT	ENSP00000368368.3:p.Leu294=
ENST00000379079.6:c.246_247delinsAT	ENSP00000368370.2:p.Leu82=
ENST00000448076.7:c.882_883delinsAT	ENSP00000413452.3:p.Leu294=
ENST00000452863.7:c.882_883delinsAT	ENSP00000415516.3:p.Leu294=
ENST00000527775.1:c.135_136delinsAT	ENSP00000435351.1:p.Leu45=
ENST00000530998.5:c.246_247delinsAT	ENSP00000435307.1:p.Leu82=
NM_000378.4:c.882_883delinsAT	NP_000369.3:p.Leu294=
NM_001198551.1:c.246_247delinsAT , LRG_525t2:c.246_247delinsAT	NP_001185480.1:p.Leu82=
NM_001198552.1:c.246_247delinsAT	NP_001185481.1:p.Leu82=
NM_024424.3:c.882_883delinsAT	NP_077742.2:p.Leu294=
NM_024426.4:c.882_883delinsAT	NP_077744.3:p.Leu294=
NM_000378.5:c.897_898delinsAT	NP_000369.4:p.Leu299=
NM_024424.4:c.897_898delinsAT	NP_077742.3:p.Leu299=
NM_024426.5:c.897_898delinsAT	NP_077744.4:p.Leu299=
NR_160306.1:n.1076_1077delinsAT
NM_000378.6:c.897_898delinsAT	NP_000369.4:p.Leu299=
NM_001198552.2:c.246_247delinsAT	NP_001185481.1:p.Leu82=
NM_024424.5:c.897_898delinsAT	NP_077742.3:p.Leu299=
NM_024426.6:c.897_898delinsAT MANE Select	NP_077744.4:p.Leu299=