Canonical Allele Identifier: CA473182187

Gene: WEE1

Linked Data

• MyVariant Identifiers: chr11:g.9607044T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9585497T>C , CM000673.2:g.9585497T>C	GRCh38
NC_000011.9:g.9607044T>C , CM000673.1:g.9607044T>C	GRCh37
NC_000011.8:g.9563620T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000450114.7:c.1440T>C MANE Select	ENSP00000402084.2:p.Ser480=
ENST00000530712.6:c.258T>C	ENSP00000434148.2:p.Ser86=
ENST00000680141.1:c.*390T>C	ENSP00000506686.1:n.*390T>C
ENST00000681684.1:c.798T>C	ENSP00000506667.1:p.Ser266=
ENST00000299613.10:c.798T>C	ENSP00000299613.5:p.Ser266=
ENST00000450114.6:c.1440T>C	ENSP00000402084.2:p.Ser480=
ENST00000524612.5:c.324T>C	ENSP00000434446.1:p.Ser108=
ENST00000530175.5:c.287T>C
ENST00000530712.5:c.258T>C	ENSP00000434148.1:p.Ser86=
ENST00000532275.1:n.227T>C
NM_001143976.1:c.798T>C	NP_001137448.1:p.Ser266=
NM_003390.3:c.1440T>C	NP_003381.1:p.Ser480=
XM_005253118.3:c.1440T>C	XP_005253175.1:p.Ser480=
XM_005253119.3:c.798T>C	XP_005253176.1:p.Ser266=
NM_003390.4:c.1440T>C MANE Select	NP_003381.1:p.Ser480=
NM_001143976.2:c.798T>C	NP_001137448.1:p.Ser266=