Canonical Allele Identifier: CA1548139346
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56881886A= , CM000667.2:g.56881886A= GRCh38
NC_000005.9:g.56177713A= , CM000667.1:g.56177713A= GRCh37
NC_000005.8:g.56213470A= NCBI36
NG_031884.1:g.71814A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.2686A= MANE Select ENSP00000382423.3:p.Thr896=
ENST00000399503.3:c.2686A= ENSP00000382423.3:p.Thr896=
NM_005921.1:c.2686A= NP_005912.1:p.Thr896=
XM_005248519.3:c.2308A= XP_005248576.2:p.Thr770=
XM_011543406.1:c.2431A= XP_011541708.1:p.Thr811=
XM_011543407.1:c.2407A= XP_011541709.1:p.Thr803=
XM_011543408.1:c.2686A= XP_011541710.1:p.Thr896=
XM_017009484.1:c.2275A= XP_016864973.1:p.Thr759=
XM_017009485.1:c.2197A= XP_016864974.1:p.Thr733=
XR_001742068.2:n.2717A=
NM_005921.2:c.2686A= MANE Select NP_005912.1:p.Thr896=