Canonical Allele Identifier: CA379848288

Gene: WEE1

Linked Data

• dbSNP Id: rs1849690922
• gnomAD v3: 11-9585499-G-A
• gnomAD v4: 11-9585499-G-A
• MyVariant Identifiers: chr11:g.9607046G>A (hg19) ; chr11:g.9585499G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9585499G>A , CM000673.2:g.9585499G>A	GRCh38
NC_000011.9:g.9607046G>A , CM000673.1:g.9607046G>A	GRCh37
NC_000011.8:g.9563622G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000450114.7:c.1442G>A MANE Select	ENSP00000402084.2:p.Arg481His
ENST00000530712.6:c.260G>A	ENSP00000434148.2:p.Arg87His
ENST00000680141.1:c.*392G>A	ENSP00000506686.1:n.*392G>A
ENST00000681684.1:c.800G>A	ENSP00000506667.1:p.Arg267His
ENST00000299613.10:c.800G>A	ENSP00000299613.5:p.Arg267His
ENST00000450114.6:c.1442G>A	ENSP00000402084.2:p.Arg481His
ENST00000524612.5:c.326G>A	ENSP00000434446.1:p.Arg109His
ENST00000530175.5:c.289G>A
ENST00000530712.5:c.260G>A	ENSP00000434148.1:p.Arg87His
ENST00000532275.1:n.229G>A
NM_001143976.1:c.800G>A	NP_001137448.1:p.Arg267His
NM_003390.3:c.1442G>A	NP_003381.1:p.Arg481His
XM_005253118.3:c.1442G>A	XP_005253175.1:p.Arg481His
XM_005253119.3:c.800G>A	XP_005253176.1:p.Arg267His
NM_003390.4:c.1442G>A MANE Select	NP_003381.1:p.Arg481His
NM_001143976.2:c.800G>A	NP_001137448.1:p.Arg267His