Canonical Allele Identifier: CA1951653077
Gene: WEE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.9585402T= , CM000673.2:g.9585402T= GRCh38
NC_000011.9:g.9606949T= , CM000673.1:g.9606949T= GRCh37
NC_000011.8:g.9563525T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000450114.7:c.1385-40T= MANE Select ENSP00000402084.2:n.1385-40T=
ENST00000530712.6:c.203-40T= ENSP00000434148.2:n.203-40T=
ENST00000680141.1:c.*335-40T= ENSP00000506686.1:n.*335-40T=
ENST00000681684.1:c.743-40T= ENSP00000506667.1:n.743-40T=
ENST00000299613.10:c.743-40T= ENSP00000299613.5:n.743-40T=
ENST00000450114.6:c.1385-40T= ENSP00000402084.2:n.1385-40T=
ENST00000524612.5:c.269-40T= ENSP00000434446.1:n.269-40T=
ENST00000530175.5:c.232-40T=
ENST00000530712.5:c.203-40T= ENSP00000434148.1:n.203-40T=
ENST00000532275.1:n.172-40T=
NM_001143976.1:c.743-40T= NP_001137448.1:n.743-40T=
NM_003390.3:c.1385-40T= NP_003381.1:n.1385-40T=
XM_005253118.3:c.1385-40T= XP_005253175.1:n.1385-40T=
XM_005253119.3:c.743-40T= XP_005253176.1:n.743-40T=
NM_003390.4:c.1385-40T= MANE Select NP_003381.1:n.1385-40T=
NM_001143976.2:c.743-40T= NP_001137448.1:n.743-40T=