Canonical Allele Identifier: CA1548136361
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56874986C= , CM000667.2:g.56874986C= GRCh38
NC_000005.9:g.56170813C= , CM000667.1:g.56170813C= GRCh37
NC_000005.8:g.56206570C= NCBI36
NG_031884.1:g.64914C=

Transcript Alleles

HGVS Amino-acid Change
NM_005921.2:c.1687-46C= MANE Select NP_005912.1:n.1687-46C=
ENST00000399503.4:c.1687-46C= MANE Select ENSP00000382423.3:n.1687-46C=
NM_005921.1:c.1687-46C= NP_005912.1:n.1687-46C=
ENST00000399503.3:c.1687-46C= ENSP00000382423.3:n.1687-46C=
XM_005248519.3:c.1309-46C= XP_005248576.2:n.1309-46C=
XM_011543406.1:c.1432-46C= XP_011541708.1:n.1432-46C=
XM_011543407.1:c.1686+1981C= XP_011541709.1:n.1686+1981C=
XM_011543408.1:c.1687-46C= XP_011541710.1:n.1687-46C=
XM_017009484.1:c.1276-46C= XP_016864973.1:n.1276-46C=
XM_017009485.1:c.1198-46C= XP_016864974.1:n.1198-46C=
XR_001742068.2:n.1718-46C=