Canonical Allele Identifier: CA1548129158
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56859670T= , CM000667.2:g.56859670T= GRCh38
NC_000005.9:g.56155497T= , CM000667.1:g.56155497T= GRCh37
NC_000005.8:g.56191254T= NCBI36
NG_031884.1:g.49598T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.634-45T= MANE Select ENSP00000382423.3:n.634-45T=
ENST00000399503.3:c.634-45T= ENSP00000382423.3:n.634-45T=
NM_005921.1:c.634-45T= NP_005912.1:n.634-45T=
XM_005248519.3:c.256-45T= XP_005248576.2:n.256-45T=
XM_011543406.1:c.379-45T= XP_011541708.1:n.379-45T=
XM_011543407.1:c.634-45T= XP_011541709.1:n.634-45T=
XM_011543408.1:c.634-45T= XP_011541710.1:n.634-45T=
XM_017009484.1:c.223-45T= XP_016864973.1:n.223-45T=
XM_017009485.1:c.145-45T= XP_016864974.1:n.145-45T=
XR_001742068.2:n.665-45T=
NM_005921.2:c.634-45T= MANE Select NP_005912.1:n.634-45T=