Canonical Allele Identifier: CA15681425
Community Standard Title: NM_003390.4(WEE1):c.1141+1133A>G
Gene: WEE1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.9578396A>G , CM000673.2:g.9578396A>G GRCh38
NC_000011.9:g.9599943A>G , CM000673.1:g.9599943A>G GRCh37
NC_000011.8:g.9556519A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_003390.4:c.1141+1133A>G MANE Select NP_003381.1:n.1141+1133A>G
ENST00000450114.7:c.1141+1133A>G MANE Select ENSP00000402084.2:n.1141+1133A>G
NM_001143976.1:c.499+1133A>G NP_001137448.1:n.499+1133A>G
NM_001143976.2:c.499+1133A>G NP_001137448.1:n.499+1133A>G
NM_003390.3:c.1141+1133A>G NP_003381.1:n.1141+1133A>G
ENST00000299613.10:c.499+1133A>G ENSP00000299613.5:n.499+1133A>G
ENST00000450114.6:c.1141+1133A>G ENSP00000402084.2:n.1141+1133A>G
ENST00000524549.1:n.2096A>G
ENST00000524612.5:c.25+501A>G ENSP00000434446.1:n.25+501A>G
ENST00000680141.1:c.*91+501A>G ENSP00000506686.1:n.*91+501A>G
ENST00000681684.1:c.499+1133A>G ENSP00000506667.1:n.499+1133A>G
XM_005253118.3:c.1141+1133A>G XP_005253175.1:n.1141+1133A>G
XM_005253119.3:c.499+1133A>G XP_005253176.1:n.499+1133A>G
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