Canonical Allele Identifier: CA1548139205
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56881521T= , CM000667.2:g.56881521T= GRCh38
NC_000005.9:g.56177348T= , CM000667.1:g.56177348T= GRCh37
NC_000005.8:g.56213105T= NCBI36
NG_031884.1:g.71449T=

Transcript Alleles

HGVS Amino-acid change
ENST00000399503.4:c.2370-49T= MANE Select ENSP00000382423.3:n.2370-49T=
ENST00000399503.3:c.2370-49T= ENSP00000382423.3:n.2370-49T=
NM_005921.1:c.2370-49T= NP_005912.1:n.2370-49T=
XM_005248519.3:c.1992-49T= XP_005248576.2:n.1992-49T=
XM_011543406.1:c.2115-49T= XP_011541708.1:n.2115-49T=
XM_011543407.1:c.2091-49T= XP_011541709.1:n.2091-49T=
XM_011543408.1:c.2370-49T= XP_011541710.1:n.2370-49T=
XM_017009484.1:c.1959-49T= XP_016864973.1:n.1959-49T=
XM_017009485.1:c.1881-49T= XP_016864974.1:n.1881-49T=
XR_001742068.2:n.2401-49T=
NM_005921.2:c.2370-49T= MANE Select NP_005912.1:n.2370-49T=