Canonical Allele Identifier: CA473182188

Gene: WEE1

Linked Data

• MyVariant Identifiers: chr11:g.9607047T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9585500T>A , CM000673.2:g.9585500T>A	GRCh38
NC_000011.9:g.9607047T>A , CM000673.1:g.9607047T>A	GRCh37
NC_000011.8:g.9563623T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000450114.7:c.1443T>A MANE Select	ENSP00000402084.2:p.Arg481=
ENST00000530712.6:c.261T>A	ENSP00000434148.2:p.Arg87=
ENST00000680141.1:c.*393T>A	ENSP00000506686.1:n.*393T>A
ENST00000681684.1:c.801T>A	ENSP00000506667.1:p.Arg267=
ENST00000299613.10:c.801T>A	ENSP00000299613.5:p.Arg267=
ENST00000450114.6:c.1443T>A	ENSP00000402084.2:p.Arg481=
ENST00000524612.5:c.327T>A	ENSP00000434446.1:p.Arg109=
ENST00000530175.5:c.290T>A
ENST00000530712.5:c.261T>A	ENSP00000434148.1:p.Arg87=
ENST00000532275.1:n.230T>A
NM_001143976.1:c.801T>A	NP_001137448.1:p.Arg267=
NM_003390.3:c.1443T>A	NP_003381.1:p.Arg481=
XM_005253118.3:c.1443T>A	XP_005253175.1:p.Arg481=
XM_005253119.3:c.801T>A	XP_005253176.1:p.Arg267=
NM_003390.4:c.1443T>A MANE Select	NP_003381.1:p.Arg481=
NM_001143976.2:c.801T>A	NP_001137448.1:p.Arg267=