Canonical Allele Identifier: CA5880015

Gene: WEE1

Linked Data

• dbSNP Id: rs769549337
• ExAC: 11:9607051 C / T
• gnomAD v2: 11-9607051-C-T
• gnomAD v4: 11-9585504-C-T
• MyVariant Identifiers: chr11:g.9607051C>T (hg19) ; chr11:g.9585504C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9585504C>T , CM000673.2:g.9585504C>T	GRCh38
NC_000011.9:g.9607051C>T , CM000673.1:g.9607051C>T	GRCh37
NC_000011.8:g.9563627C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450114.7:c.1447C>T MANE Select	ENSP00000402084.2:p.Leu483Phe
ENST00000530712.6:c.265C>T	ENSP00000434148.2:p.Leu89Phe
ENST00000680141.1:c.*397C>T	ENSP00000506686.1:n.*397C>T
ENST00000681684.1:c.805C>T	ENSP00000506667.1:p.Leu269Phe
ENST00000299613.10:c.805C>T	ENSP00000299613.5:p.Leu269Phe
ENST00000450114.6:c.1447C>T	ENSP00000402084.2:p.Leu483Phe
ENST00000524612.5:c.331C>T	ENSP00000434446.1:p.Leu111Phe
ENST00000530175.5:c.294C>T
ENST00000530712.5:c.265C>T	ENSP00000434148.1:p.Leu89Phe
ENST00000532275.1:n.234C>T
NM_001143976.1:c.805C>T	NP_001137448.1:p.Leu269Phe
NM_003390.3:c.1447C>T	NP_003381.1:p.Leu483Phe
XM_005253118.3:c.1447C>T	XP_005253175.1:p.Leu483Phe
XM_005253119.3:c.805C>T	XP_005253176.1:p.Leu269Phe
NM_003390.4:c.1447C>T MANE Select	NP_003381.1:p.Leu483Phe
NM_001143976.2:c.805C>T	NP_001137448.1:p.Leu269Phe