Canonical Allele Identifier: CA1548139287
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56881752G= , CM000667.2:g.56881752G= GRCh38
NC_000005.9:g.56177579G= , CM000667.1:g.56177579G= GRCh37
NC_000005.8:g.56213336G= NCBI36
NG_031884.1:g.71680G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.2552G= MANE Select ENSP00000382423.3:p.Arg851=
ENST00000399503.3:c.2552G= ENSP00000382423.3:p.Arg851=
NM_005921.1:c.2552G= NP_005912.1:p.Arg851=
XM_005248519.3:c.2174G= XP_005248576.2:p.Arg725=
XM_011543406.1:c.2297G= XP_011541708.1:p.Arg766=
XM_011543407.1:c.2273G= XP_011541709.1:p.Arg758=
XM_011543408.1:c.2552G= XP_011541710.1:p.Arg851=
XM_017009484.1:c.2141G= XP_016864973.1:p.Arg714=
XM_017009485.1:c.2063G= XP_016864974.1:p.Arg688=
XR_001742068.2:n.2583G=
NM_005921.2:c.2552G= MANE Select NP_005912.1:p.Arg851=