Canonical Allele Identifier: CA379848293

Gene: WEE1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450114.7:c.1444T>A MANE Select	ENSP00000402084.2:p.Phe482Ile
ENST00000530712.6:c.262T>A	ENSP00000434148.2:p.Phe88Ile
ENST00000680141.1:c.*394T>A	ENSP00000506686.1:n.*394T>A
ENST00000681684.1:c.802T>A	ENSP00000506667.1:p.Phe268Ile
ENST00000299613.10:c.802T>A	ENSP00000299613.5:p.Phe268Ile
ENST00000450114.6:c.1444T>A	ENSP00000402084.2:p.Phe482Ile
ENST00000524612.5:c.328T>A	ENSP00000434446.1:p.Phe110Ile
ENST00000530175.5:c.291T>A
ENST00000530712.5:c.262T>A	ENSP00000434148.1:p.Phe88Ile
ENST00000532275.1:n.231T>A
NM_001143976.1:c.802T>A	NP_001137448.1:p.Phe268Ile
NM_003390.3:c.1444T>A	NP_003381.1:p.Phe482Ile
XM_005253118.3:c.1444T>A	XP_005253175.1:p.Phe482Ile
XM_005253119.3:c.802T>A	XP_005253176.1:p.Phe268Ile
NM_003390.4:c.1444T>A MANE Select	NP_003381.1:p.Phe482Ile
NM_001143976.2:c.802T>A	NP_001137448.1:p.Phe268Ile