Canonical Allele Identifier: CA379848282
Gene: WEE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.9585496G>C , CM000673.2:g.9585496G>C GRCh38
NC_000011.9:g.9607043G>C , CM000673.1:g.9607043G>C GRCh37
NC_000011.8:g.9563619G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000450114.7:c.1439G>C MANE Select ENSP00000402084.2:p.Ser480Thr
ENST00000530712.6:c.257G>C ENSP00000434148.2:p.Ser86Thr
ENST00000680141.1:c.*389G>C ENSP00000506686.1:n.*389G>C
ENST00000681684.1:c.797G>C ENSP00000506667.1:p.Ser266Thr
ENST00000299613.10:c.797G>C ENSP00000299613.5:p.Ser266Thr
ENST00000450114.6:c.1439G>C ENSP00000402084.2:p.Ser480Thr
ENST00000524612.5:c.323G>C ENSP00000434446.1:p.Ser108Thr
ENST00000530175.5:c.286G>C
ENST00000530712.5:c.257G>C ENSP00000434148.1:p.Ser86Thr
ENST00000532275.1:n.226G>C
NM_001143976.1:c.797G>C NP_001137448.1:p.Ser266Thr
NM_003390.3:c.1439G>C NP_003381.1:p.Ser480Thr
XM_005253118.3:c.1439G>C XP_005253175.1:p.Ser480Thr
XM_005253119.3:c.797G>C XP_005253176.1:p.Ser266Thr
NM_003390.4:c.1439G>C MANE Select NP_003381.1:p.Ser480Thr
NM_001143976.2:c.797G>C NP_001137448.1:p.Ser266Thr