Canonical Allele Identifier: CA597424669

Gene: WEE1

Linked Data

• dbSNP Id: rs1290357461
• gnomAD v2: 11-9606949-T-C
• gnomAD v4: 11-9585402-T-C
• MyVariant Identifiers: chr11:g.9606949T>C (hg19) ; chr11:g.9585402T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9585402T>C , CM000673.2:g.9585402T>C	GRCh38
NC_000011.9:g.9606949T>C , CM000673.1:g.9606949T>C	GRCh37
NC_000011.8:g.9563525T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000450114.7:c.1385-40T>C MANE Select	ENSP00000402084.2:n.1385-40T>C
ENST00000530712.6:c.203-40T>C	ENSP00000434148.2:n.203-40T>C
ENST00000680141.1:c.*335-40T>C	ENSP00000506686.1:n.*335-40T>C
ENST00000681684.1:c.743-40T>C	ENSP00000506667.1:n.743-40T>C
ENST00000299613.10:c.743-40T>C	ENSP00000299613.5:n.743-40T>C
ENST00000450114.6:c.1385-40T>C	ENSP00000402084.2:n.1385-40T>C
ENST00000524612.5:c.269-40T>C	ENSP00000434446.1:n.269-40T>C
ENST00000530175.5:c.232-40T>C
ENST00000530712.5:c.203-40T>C	ENSP00000434148.1:n.203-40T>C
ENST00000532275.1:n.172-40T>C
NM_001143976.1:c.743-40T>C	NP_001137448.1:n.743-40T>C
NM_003390.3:c.1385-40T>C	NP_003381.1:n.1385-40T>C
XM_005253118.3:c.1385-40T>C	XP_005253175.1:n.1385-40T>C
XM_005253119.3:c.743-40T>C	XP_005253176.1:n.743-40T>C
NM_003390.4:c.1385-40T>C MANE Select	NP_003381.1:n.1385-40T>C
NM_001143976.2:c.743-40T>C	NP_001137448.1:n.743-40T>C