Canonical Allele Identifier: CA1548139570
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56882373A= , CM000667.2:g.56882373A= GRCh38
NC_000005.9:g.56178200A= , CM000667.1:g.56178200A= GRCh37
NC_000005.8:g.56213957A= NCBI36
NG_031884.1:g.72301A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.3173A= MANE Select ENSP00000382423.3:p.His1058=
ENST00000399503.3:c.3173A= ENSP00000382423.3:p.His1058=
NM_005921.1:c.3173A= NP_005912.1:p.His1058=
XM_005248519.3:c.2795A= XP_005248576.2:p.His932=
XM_011543406.1:c.2918A= XP_011541708.1:p.His973=
XM_011543407.1:c.2894A= XP_011541709.1:p.His965=
XM_011543408.1:c.3173A= XP_011541710.1:p.His1058=
XM_017009484.1:c.2762A= XP_016864973.1:p.His921=
XM_017009485.1:c.2684A= XP_016864974.1:p.His895=
XR_001742068.2:n.3204A=
NM_005921.2:c.3173A= MANE Select NP_005912.1:p.His1058=