Canonical Allele Identifier: CA5880013
Gene: WEE1 HGNC NCBI

Linked Data

dbSNP Id: rs10770042
gnomAD v2: 11-9607032-A-G
gnomAD v3: 11-9585485-A-G
gnomAD v4: 11-9585485-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.9585485A>G , CM000673.2:g.9585485A>G GRCh38
NC_000011.9:g.9607032A>G , CM000673.1:g.9607032A>G GRCh37
NC_000011.8:g.9563608A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000450114.7:c.1428A>G MANE Select ENSP00000402084.2:p.Glu476=
ENST00000530712.6:c.246A>G ENSP00000434148.2:p.Glu82=
ENST00000680141.1:c.*378A>G ENSP00000506686.1:n.*378A>G
ENST00000681684.1:c.786A>G ENSP00000506667.1:p.Glu262=
ENST00000299613.10:c.786A>G ENSP00000299613.5:p.Glu262=
ENST00000450114.6:c.1428A>G ENSP00000402084.2:p.Glu476=
ENST00000524612.5:c.312A>G ENSP00000434446.1:p.Glu104=
ENST00000530175.5:c.275A>G
ENST00000530712.5:c.246A>G ENSP00000434148.1:p.Glu82=
ENST00000532275.1:n.215A>G
NM_001143976.1:c.786A>G NP_001137448.1:p.Glu262=
NM_003390.3:c.1428A>G NP_003381.1:p.Glu476=
XM_005253118.3:c.1428A>G XP_005253175.1:p.Glu476=
XM_005253119.3:c.786A>G XP_005253176.1:p.Glu262=
NM_003390.4:c.1428A>G MANE Select NP_003381.1:p.Glu476=
NM_001143976.2:c.786A>G NP_001137448.1:p.Glu262=