Canonical Allele Identifier: CA1548139310
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56881800A= , CM000667.2:g.56881800A= GRCh38
NC_000005.9:g.56177627A= , CM000667.1:g.56177627A= GRCh37
NC_000005.8:g.56213384A= NCBI36
NG_031884.1:g.71728A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.2600A= MANE Select ENSP00000382423.3:p.Glu867=
ENST00000399503.3:c.2600A= ENSP00000382423.3:p.Glu867=
NM_005921.1:c.2600A= NP_005912.1:p.Glu867=
XM_005248519.3:c.2222A= XP_005248576.2:p.Glu741=
XM_011543406.1:c.2345A= XP_011541708.1:p.Glu782=
XM_011543407.1:c.2321A= XP_011541709.1:p.Glu774=
XM_011543408.1:c.2600A= XP_011541710.1:p.Glu867=
XM_017009484.1:c.2189A= XP_016864973.1:p.Glu730=
XM_017009485.1:c.2111A= XP_016864974.1:p.Glu704=
XR_001742068.2:n.2631A=
NM_005921.2:c.2600A= MANE Select NP_005912.1:p.Glu867=