Canonical Allele Identifier: CA1548139293
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56881763C= , CM000667.2:g.56881763C= GRCh38
NC_000005.9:g.56177590C= , CM000667.1:g.56177590C= GRCh37
NC_000005.8:g.56213347C= NCBI36
NG_031884.1:g.71691C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.2563C= MANE Select ENSP00000382423.3:p.Arg855=
ENST00000399503.3:c.2563C= ENSP00000382423.3:p.Arg855=
NM_005921.1:c.2563C= NP_005912.1:p.Arg855=
XM_005248519.3:c.2185C= XP_005248576.2:p.Arg729=
XM_011543406.1:c.2308C= XP_011541708.1:p.Arg770=
XM_011543407.1:c.2284C= XP_011541709.1:p.Arg762=
XM_011543408.1:c.2563C= XP_011541710.1:p.Arg855=
XM_017009484.1:c.2152C= XP_016864973.1:p.Arg718=
XM_017009485.1:c.2074C= XP_016864974.1:p.Arg692=
XR_001742068.2:n.2594C=
NM_005921.2:c.2563C= MANE Select NP_005912.1:p.Arg855=