Canonical Allele Identifier: CA473182195

Gene: WEE1

Linked Data

• gnomAD v4: 11-9585506-T-G
• MyVariant Identifiers: chr11:g.9607053T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9585506T>G , CM000673.2:g.9585506T>G	GRCh38
NC_000011.9:g.9607053T>G , CM000673.1:g.9607053T>G	GRCh37
NC_000011.8:g.9563629T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450114.7:c.1449T>G MANE Select	ENSP00000402084.2:p.Leu483=
ENST00000530712.6:c.267T>G	ENSP00000434148.2:p.Leu89=
ENST00000680141.1:c.*399T>G	ENSP00000506686.1:n.*399T>G
ENST00000681684.1:c.807T>G	ENSP00000506667.1:p.Leu269=
ENST00000299613.10:c.807T>G	ENSP00000299613.5:p.Leu269=
ENST00000450114.6:c.1449T>G	ENSP00000402084.2:p.Leu483=
ENST00000524612.5:c.333T>G	ENSP00000434446.1:p.Leu111=
ENST00000530175.5:c.296T>G
ENST00000530712.5:c.267T>G	ENSP00000434148.1:p.Leu89=
ENST00000532275.1:n.236T>G
NM_001143976.1:c.807T>G	NP_001137448.1:p.Leu269=
NM_003390.3:c.1449T>G	NP_003381.1:p.Leu483=
XM_005253118.3:c.1449T>G	XP_005253175.1:p.Leu483=
XM_005253119.3:c.807T>G	XP_005253176.1:p.Leu269=
NM_003390.4:c.1449T>G MANE Select	NP_003381.1:p.Leu483=
NM_001143976.2:c.807T>G	NP_001137448.1:p.Leu269=