Canonical Allele Identifier: CA379848309

Gene: WEE1

Linked Data

• MyVariant Identifiers: chr11:g.9607055C>T (hg19) ; chr11:g.9585508C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9585508C>T , CM000673.2:g.9585508C>T	GRCh38
NC_000011.9:g.9607055C>T , CM000673.1:g.9607055C>T	GRCh37
NC_000011.8:g.9563631C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450114.7:c.1451C>T MANE Select	ENSP00000402084.2:p.Ala484Val
ENST00000530712.6:c.269C>T	ENSP00000434148.2:p.Ala90Val
ENST00000680141.1:c.*401C>T	ENSP00000506686.1:n.*401C>T
ENST00000681684.1:c.809C>T	ENSP00000506667.1:p.Ala270Val
ENST00000299613.10:c.809C>T	ENSP00000299613.5:p.Ala270Val
ENST00000450114.6:c.1451C>T	ENSP00000402084.2:p.Ala484Val
ENST00000524612.5:c.335C>T	ENSP00000434446.1:p.Ala112Val
ENST00000530175.5:c.298C>T
ENST00000530712.5:c.269C>T	ENSP00000434148.1:p.Ala90Val
ENST00000532275.1:n.238C>T
NM_001143976.1:c.809C>T	NP_001137448.1:p.Ala270Val
NM_003390.3:c.1451C>T	NP_003381.1:p.Ala484Val
XM_005253118.3:c.1451C>T	XP_005253175.1:p.Ala484Val
XM_005253119.3:c.809C>T	XP_005253176.1:p.Ala270Val
NM_003390.4:c.1451C>T MANE Select	NP_003381.1:p.Ala484Val
NM_001143976.2:c.809C>T	NP_001137448.1:p.Ala270Val