Canonical Allele Identifier: CA379848281

Gene: WEE1

Linked Data

• MyVariant Identifiers: chr11:g.9607043G>A (hg19) ; chr11:g.9585496G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9585496G>A , CM000673.2:g.9585496G>A	GRCh38
NC_000011.9:g.9607043G>A , CM000673.1:g.9607043G>A	GRCh37
NC_000011.8:g.9563619G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000450114.7:c.1439G>A MANE Select	ENSP00000402084.2:p.Ser480Asn
ENST00000530712.6:c.257G>A	ENSP00000434148.2:p.Ser86Asn
ENST00000680141.1:c.*389G>A	ENSP00000506686.1:n.*389G>A
ENST00000681684.1:c.797G>A	ENSP00000506667.1:p.Ser266Asn
ENST00000299613.10:c.797G>A	ENSP00000299613.5:p.Ser266Asn
ENST00000450114.6:c.1439G>A	ENSP00000402084.2:p.Ser480Asn
ENST00000524612.5:c.323G>A	ENSP00000434446.1:p.Ser108Asn
ENST00000530175.5:c.286G>A
ENST00000530712.5:c.257G>A	ENSP00000434148.1:p.Ser86Asn
ENST00000532275.1:n.226G>A
NM_001143976.1:c.797G>A	NP_001137448.1:p.Ser266Asn
NM_003390.3:c.1439G>A	NP_003381.1:p.Ser480Asn
XM_005253118.3:c.1439G>A	XP_005253175.1:p.Ser480Asn
XM_005253119.3:c.797G>A	XP_005253176.1:p.Ser266Asn
NM_003390.4:c.1439G>A MANE Select	NP_003381.1:p.Ser480Asn
NM_001143976.2:c.797G>A	NP_001137448.1:p.Ser266Asn