Canonical Allele Identifier: CA1951653212
Gene: WEE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.9585491C= , CM000673.2:g.9585491C= GRCh38
NC_000011.9:g.9607038C= , CM000673.1:g.9607038C= GRCh37
NC_000011.8:g.9563614C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000450114.7:c.1434C= MANE Select ENSP00000402084.2:p.Gly478=
ENST00000530712.6:c.252C= ENSP00000434148.2:p.Gly84=
ENST00000680141.1:c.*384C= ENSP00000506686.1:n.*384C=
ENST00000681684.1:c.792C= ENSP00000506667.1:p.Gly264=
ENST00000299613.10:c.792C= ENSP00000299613.5:p.Gly264=
ENST00000450114.6:c.1434C= ENSP00000402084.2:p.Gly478=
ENST00000524612.5:c.318C= ENSP00000434446.1:p.Gly106=
ENST00000530175.5:c.281C=
ENST00000530712.5:c.252C= ENSP00000434148.1:p.Gly84=
ENST00000532275.1:n.221C=
NM_001143976.1:c.792C= NP_001137448.1:p.Gly264=
NM_003390.3:c.1434C= NP_003381.1:p.Gly478=
XM_005253118.3:c.1434C= XP_005253175.1:p.Gly478=
XM_005253119.3:c.792C= XP_005253176.1:p.Gly264=
NM_003390.4:c.1434C= MANE Select NP_003381.1:p.Gly478=
NM_001143976.2:c.792C= NP_001137448.1:p.Gly264=