Canonical Allele Identifier: CA1548129225
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56859826C= , CM000667.2:g.56859826C= GRCh38
NC_000005.9:g.56155653C= , CM000667.1:g.56155653C= GRCh37
NC_000005.8:g.56191410C= NCBI36
NG_031884.1:g.49754C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.745C= MANE Select ENSP00000382423.3:p.Arg249=
ENST00000399503.3:c.745C= ENSP00000382423.3:p.Arg249=
NM_005921.1:c.745C= NP_005912.1:p.Arg249=
XM_005248519.3:c.367C= XP_005248576.2:p.Arg123=
XM_011543406.1:c.490C= XP_011541708.1:p.Arg164=
XM_011543407.1:c.745C= XP_011541709.1:p.Arg249=
XM_011543408.1:c.745C= XP_011541710.1:p.Arg249=
XM_017009484.1:c.334C= XP_016864973.1:p.Arg112=
XM_017009485.1:c.256C= XP_016864974.1:p.Arg86=
XR_001742068.2:n.776C=
NM_005921.2:c.745C= MANE Select NP_005912.1:p.Arg249=