Canonical Allele Identifier: CA1548139505
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56882217T= , CM000667.2:g.56882217T= GRCh38
NC_000005.9:g.56178044T= , CM000667.1:g.56178044T= GRCh37
NC_000005.8:g.56213801T= NCBI36
NG_031884.1:g.72145T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.3017T= MANE Select ENSP00000382423.3:p.Leu1006=
ENST00000399503.3:c.3017T= ENSP00000382423.3:p.Leu1006=
NM_005921.1:c.3017T= NP_005912.1:p.Leu1006=
XM_005248519.3:c.2639T= XP_005248576.2:p.Leu880=
XM_011543406.1:c.2762T= XP_011541708.1:p.Leu921=
XM_011543407.1:c.2738T= XP_011541709.1:p.Leu913=
XM_011543408.1:c.3017T= XP_011541710.1:p.Leu1006=
XM_017009484.1:c.2606T= XP_016864973.1:p.Leu869=
XM_017009485.1:c.2528T= XP_016864974.1:p.Leu843=
XR_001742068.2:n.3048T=
NM_005921.2:c.3017T= MANE Select NP_005912.1:p.Leu1006=