Canonical Allele Identifier: CA379848255

Gene: WEE1

Linked Data

• MyVariant Identifiers: chr11:g.9607032A>T (hg19) ; chr11:g.9585485A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9585485A>T , CM000673.2:g.9585485A>T	GRCh38
NC_000011.9:g.9607032A>T , CM000673.1:g.9607032A>T	GRCh37
NC_000011.8:g.9563608A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000450114.7:c.1428A>T MANE Select	ENSP00000402084.2:p.Glu476Asp
ENST00000530712.6:c.246A>T	ENSP00000434148.2:p.Glu82Asp
ENST00000680141.1:c.*378A>T	ENSP00000506686.1:n.*378A>T
ENST00000681684.1:c.786A>T	ENSP00000506667.1:p.Glu262Asp
ENST00000299613.10:c.786A>T	ENSP00000299613.5:p.Glu262Asp
ENST00000450114.6:c.1428A>T	ENSP00000402084.2:p.Glu476Asp
ENST00000524612.5:c.312A>T	ENSP00000434446.1:p.Glu104Asp
ENST00000530175.5:c.275A>T
ENST00000530712.5:c.246A>T	ENSP00000434148.1:p.Glu82Asp
ENST00000532275.1:n.215A>T
NM_001143976.1:c.786A>T	NP_001137448.1:p.Glu262Asp
NM_003390.3:c.1428A>T	NP_003381.1:p.Glu476Asp
XM_005253118.3:c.1428A>T	XP_005253175.1:p.Glu476Asp
XM_005253119.3:c.786A>T	XP_005253176.1:p.Glu262Asp
NM_003390.4:c.1428A>T MANE Select	NP_003381.1:p.Glu476Asp
NM_001143976.2:c.786A>T	NP_001137448.1:p.Glu262Asp