Canonical Allele Identifier: CA5880005

Gene: WEE1

Linked Data

• dbSNP Id: rs756597519
• ExAC: 11:9606979 A / G
• gnomAD v2: 11-9606979-A-G
• gnomAD v3: 11-9585432-A-G
• gnomAD v4: 11-9585432-A-G
• MyVariant Identifiers: chr11:g.9606979A>G (hg19) ; chr11:g.9585432A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9585432A>G , CM000673.2:g.9585432A>G	GRCh38
NC_000011.9:g.9606979A>G , CM000673.1:g.9606979A>G	GRCh37
NC_000011.8:g.9563555A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450114.7:c.1385-10A>G MANE Select	ENSP00000402084.2:n.1385-10A>G
ENST00000530712.6:c.203-10A>G	ENSP00000434148.2:n.203-10A>G
ENST00000680141.1:c.*335-10A>G	ENSP00000506686.1:n.*335-10A>G
ENST00000681684.1:c.743-10A>G	ENSP00000506667.1:n.743-10A>G
ENST00000299613.10:c.743-10A>G	ENSP00000299613.5:n.743-10A>G
ENST00000450114.6:c.1385-10A>G	ENSP00000402084.2:n.1385-10A>G
ENST00000524612.5:c.269-10A>G	ENSP00000434446.1:n.269-10A>G
ENST00000530175.5:c.232-10A>G
ENST00000530712.5:c.203-10A>G	ENSP00000434148.1:n.203-10A>G
ENST00000532275.1:n.172-10A>G
NM_001143976.1:c.743-10A>G	NP_001137448.1:n.743-10A>G
NM_003390.3:c.1385-10A>G	NP_003381.1:n.1385-10A>G
XM_005253118.3:c.1385-10A>G	XP_005253175.1:n.1385-10A>G
XM_005253119.3:c.743-10A>G	XP_005253176.1:n.743-10A>G
NM_003390.4:c.1385-10A>G MANE Select	NP_003381.1:n.1385-10A>G
NM_001143976.2:c.743-10A>G	NP_001137448.1:n.743-10A>G