Canonical Allele Identifier: CA1548136396
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56875101C= , CM000667.2:g.56875101C= GRCh38
NC_000005.9:g.56170928C= , CM000667.1:g.56170928C= GRCh37
NC_000005.8:g.56206685C= NCBI36
NG_031884.1:g.65029C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.1756C= MANE Select ENSP00000382423.3:p.Arg586=
ENST00000399503.3:c.1756C= ENSP00000382423.3:p.Arg586=
NM_005921.1:c.1756C= NP_005912.1:p.Arg586=
XM_005248519.3:c.1378C= XP_005248576.2:p.Arg460=
XM_011543406.1:c.1501C= XP_011541708.1:p.Arg501=
XM_011543407.1:c.1686+2096C= XP_011541709.1:n.1686+2096C=
XM_011543408.1:c.1756C= XP_011541710.1:p.Arg586=
XM_017009484.1:c.1345C= XP_016864973.1:p.Arg449=
XM_017009485.1:c.1267C= XP_016864974.1:p.Arg423=
XR_001742068.2:n.1787C=
NM_005921.2:c.1756C= MANE Select NP_005912.1:p.Arg586=