Canonical Allele Identifier: CA2673908359
Gene: MAP3K1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56859908del , CM000667.2:g.56859908del GRCh38
NC_000005.9:g.56155735del , CM000667.1:g.56155735del GRCh37
NC_000005.8:g.56191492del NCBI36
NG_031884.1:g.49836del

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.827del MANE Select ENSP00000382423.3:p.Pro276GlnfsTer?
ENST00000399503.3:c.827del ENSP00000382423.3:p.Pro276GlnfsTer?
NM_005921.1:c.827del NP_005912.1:p.Pro276GlnfsTer?
XM_005248519.3:c.449del XP_005248576.2:p.Pro150GlnfsTer?
XM_011543406.1:c.572del XP_011541708.1:p.Pro191GlnfsTer?
XM_011543407.1:c.827del XP_011541709.1:p.Pro276GlnfsTer?
XM_011543408.1:c.827del XP_011541710.1:p.Pro276GlnfsTer?
XM_017009484.1:c.416del XP_016864973.1:p.Pro139GlnfsTer?
XM_017009485.1:c.338del XP_016864974.1:p.Pro113GlnfsTer?
XR_001742068.2:n.858del
NM_005921.2:c.827del MANE Select NP_005912.1:p.Pro276GlnfsTer?