Canonical Allele Identifier: CA5880016

Gene: WEE1

Linked Data

• dbSNP Id: rs773071613
• ExAC: 11:9607058 A / G
• gnomAD v2: 11-9607058-A-G
• gnomAD v4: 11-9585511-A-G
• MyVariant Identifiers: chr11:g.9607058A>G (hg19) ; chr11:g.9585511A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9585511A>G , CM000673.2:g.9585511A>G	GRCh38
NC_000011.9:g.9607058A>G , CM000673.1:g.9607058A>G	GRCh37
NC_000011.8:g.9563634A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000450114.7:c.1454A>G MANE Select	ENSP00000402084.2:p.Asn485Ser
ENST00000530712.6:c.272A>G	ENSP00000434148.2:p.Asn91Ser
ENST00000680141.1:c.*404A>G	ENSP00000506686.1:n.*404A>G
ENST00000681684.1:c.812A>G	ENSP00000506667.1:p.Asn271Ser
ENST00000299613.10:c.812A>G	ENSP00000299613.5:p.Asn271Ser
ENST00000450114.6:c.1454A>G	ENSP00000402084.2:p.Asn485Ser
ENST00000524612.5:c.338A>G	ENSP00000434446.1:p.Asn113Ser
ENST00000530175.5:c.301A>G
ENST00000530712.5:c.272A>G	ENSP00000434148.1:p.Asn91Ser
ENST00000532275.1:n.241A>G
NM_001143976.1:c.812A>G	NP_001137448.1:p.Asn271Ser
NM_003390.3:c.1454A>G	NP_003381.1:p.Asn485Ser
XM_005253118.3:c.1454A>G	XP_005253175.1:p.Asn485Ser
XM_005253119.3:c.812A>G	XP_005253176.1:p.Asn271Ser
NM_003390.4:c.1454A>G MANE Select	NP_003381.1:p.Asn485Ser
NM_001143976.2:c.812A>G	NP_001137448.1:p.Asn271Ser