Canonical Allele Identifier: CA379848316

Gene: WEE1

Linked Data

• MyVariant Identifiers: chr11:g.9607059T>G (hg19) ; chr11:g.9585512T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9585512T>G , CM000673.2:g.9585512T>G	GRCh38
NC_000011.9:g.9607059T>G , CM000673.1:g.9607059T>G	GRCh37
NC_000011.8:g.9563635T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000450114.7:c.1455T>G MANE Select	ENSP00000402084.2:p.Asn485Lys
ENST00000530712.6:c.273T>G	ENSP00000434148.2:p.Asn91Lys
ENST00000680141.1:c.*405T>G	ENSP00000506686.1:n.*405T>G
ENST00000681684.1:c.813T>G	ENSP00000506667.1:p.Asn271Lys
ENST00000299613.10:c.813T>G	ENSP00000299613.5:p.Asn271Lys
ENST00000450114.6:c.1455T>G	ENSP00000402084.2:p.Asn485Lys
ENST00000524612.5:c.339T>G	ENSP00000434446.1:p.Asn113Lys
ENST00000530175.5:c.302T>G
ENST00000530712.5:c.273T>G	ENSP00000434148.1:p.Asn91Lys
ENST00000532275.1:n.242T>G
NM_001143976.1:c.813T>G	NP_001137448.1:p.Asn271Lys
NM_003390.3:c.1455T>G	NP_003381.1:p.Asn485Lys
XM_005253118.3:c.1455T>G	XP_005253175.1:p.Asn485Lys
XM_005253119.3:c.813T>G	XP_005253176.1:p.Asn271Lys
NM_003390.4:c.1455T>G MANE Select	NP_003381.1:p.Asn485Lys
NM_001143976.2:c.813T>G	NP_001137448.1:p.Asn271Lys