Canonical Allele Identifier: CA379960359

Gene: WT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32399984G>C , CM000673.2:g.32399984G>C	GRCh38
NC_000011.9:g.32421530G>C , CM000673.1:g.32421530G>C	GRCh37
NC_000011.8:g.32378106G>C	NCBI36
NG_009272.1:g.40558C>G , LRG_525:g.40558C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_024426.6:c.1077C>G MANE Select	NP_077744.4:p.Tyr359Ter
ENST00000452863.10:c.1077C>G MANE Select	ENSP00000415516.5:p.Tyr359Ter
NM_000378.4:c.1011C>G	NP_000369.3:p.Tyr337Ter
NM_000378.5:c.1026C>G	NP_000369.4:p.Tyr342Ter
NM_000378.6:c.1026C>G	NP_000369.4:p.Tyr342Ter
NM_001198551.1:c.426C>G , LRG_525t2:c.426C>G	NP_001185480.1:p.Tyr142Ter
NM_001198552.1:c.375C>G	NP_001185481.1:p.Tyr125Ter
NM_001198552.2:c.375C>G	NP_001185481.1:p.Tyr125Ter
NM_001367854.1:c.-112C>G	NP_001354783.1:n.-112C>G
NM_024424.3:c.1062C>G	NP_077742.2:p.Tyr354Ter
NM_024424.4:c.1077C>G	NP_077742.3:p.Tyr359Ter
NM_024424.5:c.1077C>G	NP_077742.3:p.Tyr359Ter
NM_024426.4:c.1062C>G	NP_077744.3:p.Tyr354Ter
NM_024426.5:c.1077C>G	NP_077744.4:p.Tyr359Ter
NR_160306.1:n.1409C>G
ENST00000332351.7:c.1062C>G	ENSP00000331327.3:p.Tyr354Ter
ENST00000332351.9:c.1026C>G	ENSP00000331327.5:p.Tyr342Ter
ENST00000379077.7:c.*261C>G	ENSP00000368368.3:n.*261C>G
ENST00000379077.9:c.*261C>G	ENSP00000368368.5:n.*261C>G
ENST00000379079.6:c.426C>G	ENSP00000368370.2:p.Tyr142Ter
ENST00000379079.8:c.426C>G	ENSP00000368370.2:p.Tyr142Ter
ENST00000448076.7:c.1062C>G	ENSP00000413452.3:p.Tyr354Ter
ENST00000448076.9:c.1077C>G	ENSP00000413452.5:p.Tyr359Ter
ENST00000452863.7:c.1011C>G	ENSP00000415516.3:p.Tyr337Ter
ENST00000526685.1:c.-112C>G	ENSP00000436292.1:n.-112C>G
ENST00000526685.2:n.531C>G
ENST00000527775.1:c.315C>G	ENSP00000435351.1:p.Tyr105Ter
ENST00000527882.5:c.133C>G
ENST00000530998.5:c.375C>G	ENSP00000435307.1:p.Tyr125Ter
ENST00000639563.3:c.1026C>G	ENSP00000492269.3:p.Tyr342Ter
ENST00000639907.2:n.220C>G
ENST00000640146.2:c.402C>G	ENSP00000491984.2:p.Tyr134Ter
ENST00000651794.1:n.820C>G
ENST00000652579.1:n.237C>G
ENST00000652724.1:n.267C>G