Canonical Allele Identifier: CA1548129260
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56859891G= , CM000667.2:g.56859891G= GRCh38
NC_000005.9:g.56155718G= , CM000667.1:g.56155718G= GRCh37
NC_000005.8:g.56191475G= NCBI36
NG_031884.1:g.49819G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.810G= MANE Select ENSP00000382423.3:p.Arg270=
ENST00000399503.3:c.810G= ENSP00000382423.3:p.Arg270=
NM_005921.1:c.810G= NP_005912.1:p.Arg270=
XM_005248519.3:c.432G= XP_005248576.2:p.Arg144=
XM_011543406.1:c.555G= XP_011541708.1:p.Arg185=
XM_011543407.1:c.810G= XP_011541709.1:p.Arg270=
XM_011543408.1:c.810G= XP_011541710.1:p.Arg270=
XM_017009484.1:c.399G= XP_016864973.1:p.Arg133=
XM_017009485.1:c.321G= XP_016864974.1:p.Arg107=
XR_001742068.2:n.841G=
NM_005921.2:c.810G= MANE Select NP_005912.1:p.Arg270=