Canonical Allele Identifier: CA2708944151
Gene: MAP3K1 HGNC NCBI

Linked Data

dbSNP Id: rs2111874704

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56859898del , CM000667.2:g.56859898del GRCh38
NC_000005.9:g.56155725del , CM000667.1:g.56155725del GRCh37
NC_000005.8:g.56191482del NCBI36
NG_031884.1:g.49826del

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.817del MANE Select ENSP00000382423.3:p.Arg273GlufsTer?
ENST00000399503.3:c.817del ENSP00000382423.3:p.Arg273GlufsTer?
NM_005921.1:c.817del NP_005912.1:p.Arg273GlufsTer?
XM_005248519.3:c.439del XP_005248576.2:p.Arg147GlufsTer?
XM_011543406.1:c.562del XP_011541708.1:p.Arg188GlufsTer?
XM_011543407.1:c.817del XP_011541709.1:p.Arg273GlufsTer?
XM_011543408.1:c.817del XP_011541710.1:p.Arg273GlufsTer?
XM_017009484.1:c.406del XP_016864973.1:p.Arg136GlufsTer?
XM_017009485.1:c.328del XP_016864974.1:p.Arg110GlufsTer?
XR_001742068.2:n.848del
NM_005921.2:c.817del MANE Select NP_005912.1:p.Arg273GlufsTer?