Canonical Allele Identifier: CA1951653122

Gene: WEE1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9585435C= , CM000673.2:g.9585435C=	GRCh38
NC_000011.9:g.9606982C= , CM000673.1:g.9606982C=	GRCh37
NC_000011.8:g.9563558C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450114.7:c.1385-7C= MANE Select	ENSP00000402084.2:n.1385-7C=
ENST00000530712.6:c.203-7C=	ENSP00000434148.2:n.203-7C=
ENST00000680141.1:c.*335-7C=	ENSP00000506686.1:n.*335-7C=
ENST00000681684.1:c.743-7C=	ENSP00000506667.1:n.743-7C=
ENST00000299613.10:c.743-7C=	ENSP00000299613.5:n.743-7C=
ENST00000450114.6:c.1385-7C=	ENSP00000402084.2:n.1385-7C=
ENST00000524612.5:c.269-7C=	ENSP00000434446.1:n.269-7C=
ENST00000530175.5:c.232-7C=
ENST00000530712.5:c.203-7C=	ENSP00000434148.1:n.203-7C=
ENST00000532275.1:n.172-7C=
NM_001143976.1:c.743-7C=	NP_001137448.1:n.743-7C=
NM_003390.3:c.1385-7C=	NP_003381.1:n.1385-7C=
XM_005253118.3:c.1385-7C=	XP_005253175.1:n.1385-7C=
XM_005253119.3:c.743-7C=	XP_005253176.1:n.743-7C=
NM_003390.4:c.1385-7C= MANE Select	NP_003381.1:n.1385-7C=
NM_001143976.2:c.743-7C=	NP_001137448.1:n.743-7C=