Canonical Allele Identifier: CA1548129212
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56859798T= , CM000667.2:g.56859798T= GRCh38
NC_000005.9:g.56155625T= , CM000667.1:g.56155625T= GRCh37
NC_000005.8:g.56191382T= NCBI36
NG_031884.1:g.49726T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.717T= MANE Select ENSP00000382423.3:p.Ser239=
ENST00000399503.3:c.717T= ENSP00000382423.3:p.Ser239=
NM_005921.1:c.717T= NP_005912.1:p.Ser239=
XM_005248519.3:c.339T= XP_005248576.2:p.Ser113=
XM_011543406.1:c.462T= XP_011541708.1:p.Ser154=
XM_011543407.1:c.717T= XP_011541709.1:p.Ser239=
XM_011543408.1:c.717T= XP_011541710.1:p.Ser239=
XM_017009484.1:c.306T= XP_016864973.1:p.Ser102=
XM_017009485.1:c.228T= XP_016864974.1:p.Ser76=
XR_001742068.2:n.748T=
NM_005921.2:c.717T= MANE Select NP_005912.1:p.Ser239=