Canonical Allele Identifier: CA645557009
Gene: MAP3K1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56881830del , CM000667.2:g.56881830del GRCh38
NC_000005.9:g.56177657del , CM000667.1:g.56177657del GRCh37
NC_000005.8:g.56213414del NCBI36
NG_031884.1:g.71758del

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.2630del MANE Select ENSP00000382423.3:p.Leu877TrpfsTer?
ENST00000399503.3:c.2630del ENSP00000382423.3:p.Leu877TrpfsTer?
NM_005921.1:c.2630del NP_005912.1:p.Leu877TrpfsTer?
XM_005248519.3:c.2252del XP_005248576.2:p.Leu751TrpfsTer?
XM_011543406.1:c.2375del XP_011541708.1:p.Leu792TrpfsTer?
XM_011543407.1:c.2351del XP_011541709.1:p.Leu784TrpfsTer?
XM_011543408.1:c.2630del XP_011541710.1:p.Leu877TrpfsTer?
XM_017009484.1:c.2219del XP_016864973.1:p.Leu740TrpfsTer?
XM_017009485.1:c.2141del XP_016864974.1:p.Leu714TrpfsTer?
XR_001742068.2:n.2661del
NM_005921.2:c.2630del MANE Select NP_005912.1:p.Leu877TrpfsTer?