Canonical Allele Identifier: CA1548139524
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56882260A= , CM000667.2:g.56882260A= GRCh38
NC_000005.9:g.56178087A= , CM000667.1:g.56178087A= GRCh37
NC_000005.8:g.56213844A= NCBI36
NG_031884.1:g.72188A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.3060A= MANE Select ENSP00000382423.3:p.Gln1020=
ENST00000399503.3:c.3060A= ENSP00000382423.3:p.Gln1020=
NM_005921.1:c.3060A= NP_005912.1:p.Gln1020=
XM_005248519.3:c.2682A= XP_005248576.2:p.Gln894=
XM_011543406.1:c.2805A= XP_011541708.1:p.Gln935=
XM_011543407.1:c.2781A= XP_011541709.1:p.Gln927=
XM_011543408.1:c.3060A= XP_011541710.1:p.Gln1020=
XM_017009484.1:c.2649A= XP_016864973.1:p.Gln883=
XM_017009485.1:c.2571A= XP_016864974.1:p.Gln857=
XR_001742068.2:n.3091A=
NM_005921.2:c.3060A= MANE Select NP_005912.1:p.Gln1020=