Canonical Allele Identifier: CA1951653228

Gene: WEE1

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450114.7:c.1454A= MANE Select	ENSP00000402084.2:p.Asn485=
ENST00000530712.6:c.272A=	ENSP00000434148.2:p.Asn91=
ENST00000680141.1:c.*404A=	ENSP00000506686.1:n.*404A=
ENST00000681684.1:c.812A=	ENSP00000506667.1:p.Asn271=
ENST00000299613.10:c.812A=	ENSP00000299613.5:p.Asn271=
ENST00000450114.6:c.1454A=	ENSP00000402084.2:p.Asn485=
ENST00000524612.5:c.338A=	ENSP00000434446.1:p.Asn113=
ENST00000530175.5:c.301A=
ENST00000530712.5:c.272A=	ENSP00000434148.1:p.Asn91=
ENST00000532275.1:n.241A=
NM_001143976.1:c.812A=	NP_001137448.1:p.Asn271=
NM_003390.3:c.1454A=	NP_003381.1:p.Asn485=
XM_005253118.3:c.1454A=	XP_005253175.1:p.Asn485=
XM_005253119.3:c.812A=	XP_005253176.1:p.Asn271=
NM_003390.4:c.1454A= MANE Select	NP_003381.1:p.Asn485=
NM_001143976.2:c.812A=	NP_001137448.1:p.Asn271=