Canonical Allele Identifier: CA379848259

Gene: WEE1

Linked Data

• MyVariant Identifiers: chr11:g.9607034A>C (hg19) ; chr11:g.9585487A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9585487A>C , CM000673.2:g.9585487A>C	GRCh38
NC_000011.9:g.9607034A>C , CM000673.1:g.9607034A>C	GRCh37
NC_000011.8:g.9563610A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000450114.7:c.1430A>C MANE Select	ENSP00000402084.2:p.Glu477Ala
ENST00000530712.6:c.248A>C	ENSP00000434148.2:p.Glu83Ala
ENST00000680141.1:c.*380A>C	ENSP00000506686.1:n.*380A>C
ENST00000681684.1:c.788A>C	ENSP00000506667.1:p.Glu263Ala
ENST00000299613.10:c.788A>C	ENSP00000299613.5:p.Glu263Ala
ENST00000450114.6:c.1430A>C	ENSP00000402084.2:p.Glu477Ala
ENST00000524612.5:c.314A>C	ENSP00000434446.1:p.Glu105Ala
ENST00000530175.5:c.277A>C
ENST00000530712.5:c.248A>C	ENSP00000434148.1:p.Glu83Ala
ENST00000532275.1:n.217A>C
NM_001143976.1:c.788A>C	NP_001137448.1:p.Glu263Ala
NM_003390.3:c.1430A>C	NP_003381.1:p.Glu477Ala
XM_005253118.3:c.1430A>C	XP_005253175.1:p.Glu477Ala
XM_005253119.3:c.788A>C	XP_005253176.1:p.Glu263Ala
NM_003390.4:c.1430A>C MANE Select	NP_003381.1:p.Glu477Ala
NM_001143976.2:c.788A>C	NP_001137448.1:p.Glu263Ala