Canonical Allele Identifier: CA379848292

Gene: WEE1

Linked Data

• MyVariant Identifiers: chr11:g.9607048T>C (hg19) ; chr11:g.9585501T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9585501T>C , CM000673.2:g.9585501T>C	GRCh38
NC_000011.9:g.9607048T>C , CM000673.1:g.9607048T>C	GRCh37
NC_000011.8:g.9563624T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450114.7:c.1444T>C MANE Select	ENSP00000402084.2:p.Phe482Leu
ENST00000530712.6:c.262T>C	ENSP00000434148.2:p.Phe88Leu
ENST00000680141.1:c.*394T>C	ENSP00000506686.1:n.*394T>C
ENST00000681684.1:c.802T>C	ENSP00000506667.1:p.Phe268Leu
ENST00000299613.10:c.802T>C	ENSP00000299613.5:p.Phe268Leu
ENST00000450114.6:c.1444T>C	ENSP00000402084.2:p.Phe482Leu
ENST00000524612.5:c.328T>C	ENSP00000434446.1:p.Phe110Leu
ENST00000530175.5:c.291T>C
ENST00000530712.5:c.262T>C	ENSP00000434148.1:p.Phe88Leu
ENST00000532275.1:n.231T>C
NM_001143976.1:c.802T>C	NP_001137448.1:p.Phe268Leu
NM_003390.3:c.1444T>C	NP_003381.1:p.Phe482Leu
XM_005253118.3:c.1444T>C	XP_005253175.1:p.Phe482Leu
XM_005253119.3:c.802T>C	XP_005253176.1:p.Phe268Leu
NM_003390.4:c.1444T>C MANE Select	NP_003381.1:p.Phe482Leu
NM_001143976.2:c.802T>C	NP_001137448.1:p.Phe268Leu