Canonical Allele Identifier: CA1548139305
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56881791A= , CM000667.2:g.56881791A= GRCh38
NC_000005.9:g.56177618A= , CM000667.1:g.56177618A= GRCh37
NC_000005.8:g.56213375A= NCBI36
NG_031884.1:g.71719A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.2591A= MANE Select ENSP00000382423.3:p.Glu864=
ENST00000399503.3:c.2591A= ENSP00000382423.3:p.Glu864=
NM_005921.1:c.2591A= NP_005912.1:p.Glu864=
XM_005248519.3:c.2213A= XP_005248576.2:p.Glu738=
XM_011543406.1:c.2336A= XP_011541708.1:p.Glu779=
XM_011543407.1:c.2312A= XP_011541709.1:p.Glu771=
XM_011543408.1:c.2591A= XP_011541710.1:p.Glu864=
XM_017009484.1:c.2180A= XP_016864973.1:p.Glu727=
XM_017009485.1:c.2102A= XP_016864974.1:p.Glu701=
XR_001742068.2:n.2622A=
NM_005921.2:c.2591A= MANE Select NP_005912.1:p.Glu864=