Canonical Allele Identifier: CA5879998

Gene: WEE1

Linked Data

• dbSNP Id: rs763239694
• ExAC: 11:9606937 G / C
• gnomAD v2: 11-9606937-G-C
• gnomAD v3: 11-9585390-G-C
• gnomAD v4: 11-9585390-G-C
• MyVariant Identifiers: chr11:g.9606937G>C (hg19) ; chr11:g.9585390G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9585390G>C , CM000673.2:g.9585390G>C	GRCh38
NC_000011.9:g.9606937G>C , CM000673.1:g.9606937G>C	GRCh37
NC_000011.8:g.9563513G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000450114.7:c.1384+37G>C MANE Select	ENSP00000402084.2:n.1384+37G>C
ENST00000530712.6:c.202+37G>C	ENSP00000434148.2:n.202+37G>C
ENST00000680141.1:c.*334+37G>C	ENSP00000506686.1:n.*334+37G>C
ENST00000681684.1:c.742+37G>C	ENSP00000506667.1:n.742+37G>C
ENST00000299613.10:c.742+37G>C	ENSP00000299613.5:n.742+37G>C
ENST00000450114.6:c.1384+37G>C	ENSP00000402084.2:n.1384+37G>C
ENST00000524612.5:c.268+37G>C	ENSP00000434446.1:n.268+37G>C
ENST00000530175.5:c.231+37G>C
ENST00000530712.5:c.202+37G>C	ENSP00000434148.1:n.202+37G>C
ENST00000532275.1:n.171+37G>C
NM_001143976.1:c.742+37G>C	NP_001137448.1:n.742+37G>C
NM_003390.3:c.1384+37G>C	NP_003381.1:n.1384+37G>C
XM_005253118.3:c.1384+37G>C	XP_005253175.1:n.1384+37G>C
XM_005253119.3:c.742+37G>C	XP_005253176.1:n.742+37G>C
NM_003390.4:c.1384+37G>C MANE Select	NP_003381.1:n.1384+37G>C
NM_001143976.2:c.742+37G>C	NP_001137448.1:n.742+37G>C