Canonical Allele Identifier: CA379848300

Gene: WEE1

Linked Data

• dbSNP Id: rs769549337
• gnomAD v3: 11-9585504-C-G
• gnomAD v4: 11-9585504-C-G
• MyVariant Identifiers: chr11:g.9607051C>G (hg19) ; chr11:g.9585504C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9585504C>G , CM000673.2:g.9585504C>G	GRCh38
NC_000011.9:g.9607051C>G , CM000673.1:g.9607051C>G	GRCh37
NC_000011.8:g.9563627C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000450114.7:c.1447C>G MANE Select	ENSP00000402084.2:p.Leu483Val
ENST00000530712.6:c.265C>G	ENSP00000434148.2:p.Leu89Val
ENST00000680141.1:c.*397C>G	ENSP00000506686.1:n.*397C>G
ENST00000681684.1:c.805C>G	ENSP00000506667.1:p.Leu269Val
ENST00000299613.10:c.805C>G	ENSP00000299613.5:p.Leu269Val
ENST00000450114.6:c.1447C>G	ENSP00000402084.2:p.Leu483Val
ENST00000524612.5:c.331C>G	ENSP00000434446.1:p.Leu111Val
ENST00000530175.5:c.294C>G
ENST00000530712.5:c.265C>G	ENSP00000434148.1:p.Leu89Val
ENST00000532275.1:n.234C>G
NM_001143976.1:c.805C>G	NP_001137448.1:p.Leu269Val
NM_003390.3:c.1447C>G	NP_003381.1:p.Leu483Val
XM_005253118.3:c.1447C>G	XP_005253175.1:p.Leu483Val
XM_005253119.3:c.805C>G	XP_005253176.1:p.Leu269Val
NM_003390.4:c.1447C>G MANE Select	NP_003381.1:p.Leu483Val
NM_001143976.2:c.805C>G	NP_001137448.1:p.Leu269Val