Canonical Allele Identifier: CA379848294

Gene: WEE1

Linked Data

• MyVariant Identifiers: chr11:g.9607049T>A (hg19) ; chr11:g.9585502T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9585502T>A , CM000673.2:g.9585502T>A	GRCh38
NC_000011.9:g.9607049T>A , CM000673.1:g.9607049T>A	GRCh37
NC_000011.8:g.9563625T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450114.7:c.1445T>A MANE Select	ENSP00000402084.2:p.Phe482Tyr
ENST00000530712.6:c.263T>A	ENSP00000434148.2:p.Phe88Tyr
ENST00000680141.1:c.*395T>A	ENSP00000506686.1:n.*395T>A
ENST00000681684.1:c.803T>A	ENSP00000506667.1:p.Phe268Tyr
ENST00000299613.10:c.803T>A	ENSP00000299613.5:p.Phe268Tyr
ENST00000450114.6:c.1445T>A	ENSP00000402084.2:p.Phe482Tyr
ENST00000524612.5:c.329T>A	ENSP00000434446.1:p.Phe110Tyr
ENST00000530175.5:c.292T>A
ENST00000530712.5:c.263T>A	ENSP00000434148.1:p.Phe88Tyr
ENST00000532275.1:n.232T>A
NM_001143976.1:c.803T>A	NP_001137448.1:p.Phe268Tyr
NM_003390.3:c.1445T>A	NP_003381.1:p.Phe482Tyr
XM_005253118.3:c.1445T>A	XP_005253175.1:p.Phe482Tyr
XM_005253119.3:c.803T>A	XP_005253176.1:p.Phe268Tyr
NM_003390.4:c.1445T>A MANE Select	NP_003381.1:p.Phe482Tyr
NM_001143976.2:c.803T>A	NP_001137448.1:p.Phe268Tyr