Canonical Allele Identifier: CA1951653051
Gene: WEE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.9585389A= , CM000673.2:g.9585389A= GRCh38
NC_000011.9:g.9606936A= , CM000673.1:g.9606936A= GRCh37
NC_000011.8:g.9563512A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000450114.7:c.1384+36A= MANE Select ENSP00000402084.2:n.1384+36A=
ENST00000530712.6:c.202+36A= ENSP00000434148.2:n.202+36A=
ENST00000680141.1:c.*334+36A= ENSP00000506686.1:n.*334+36A=
ENST00000681684.1:c.742+36A= ENSP00000506667.1:n.742+36A=
ENST00000299613.10:c.742+36A= ENSP00000299613.5:n.742+36A=
ENST00000450114.6:c.1384+36A= ENSP00000402084.2:n.1384+36A=
ENST00000524612.5:c.268+36A= ENSP00000434446.1:n.268+36A=
ENST00000530175.5:c.231+36A=
ENST00000530712.5:c.202+36A= ENSP00000434148.1:n.202+36A=
ENST00000532275.1:n.171+36A=
NM_001143976.1:c.742+36A= NP_001137448.1:n.742+36A=
NM_003390.3:c.1384+36A= NP_003381.1:n.1384+36A=
XM_005253118.3:c.1384+36A= XP_005253175.1:n.1384+36A=
XM_005253119.3:c.742+36A= XP_005253176.1:n.742+36A=
NM_003390.4:c.1384+36A= MANE Select NP_003381.1:n.1384+36A=
NM_001143976.2:c.742+36A= NP_001137448.1:n.742+36A=