Canonical Allele Identifier: CA1548129226
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56859827G= , CM000667.2:g.56859827G= GRCh38
NC_000005.9:g.56155654G= , CM000667.1:g.56155654G= GRCh37
NC_000005.8:g.56191411G= NCBI36
NG_031884.1:g.49755G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.746G= MANE Select ENSP00000382423.3:p.Arg249=
ENST00000399503.3:c.746G= ENSP00000382423.3:p.Arg249=
NM_005921.1:c.746G= NP_005912.1:p.Arg249=
XM_005248519.3:c.368G= XP_005248576.2:p.Arg123=
XM_011543406.1:c.491G= XP_011541708.1:p.Arg164=
XM_011543407.1:c.746G= XP_011541709.1:p.Arg249=
XM_011543408.1:c.746G= XP_011541710.1:p.Arg249=
XM_017009484.1:c.335G= XP_016864973.1:p.Arg112=
XM_017009485.1:c.257G= XP_016864974.1:p.Arg86=
XR_001742068.2:n.777G=
NM_005921.2:c.746G= MANE Select NP_005912.1:p.Arg249=