Canonical Allele Identifier: CA1548139206
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56881528G= , CM000667.2:g.56881528G= GRCh38
NC_000005.9:g.56177355G= , CM000667.1:g.56177355G= GRCh37
NC_000005.8:g.56213112G= NCBI36
NG_031884.1:g.71456G=

Transcript Alleles

HGVS Amino-acid change
ENST00000399503.4:c.2370-42G= MANE Select ENSP00000382423.3:n.2370-42G=
ENST00000399503.3:c.2370-42G= ENSP00000382423.3:n.2370-42G=
NM_005921.1:c.2370-42G= NP_005912.1:n.2370-42G=
XM_005248519.3:c.1992-42G= XP_005248576.2:n.1992-42G=
XM_011543406.1:c.2115-42G= XP_011541708.1:n.2115-42G=
XM_011543407.1:c.2091-42G= XP_011541709.1:n.2091-42G=
XM_011543408.1:c.2370-42G= XP_011541710.1:n.2370-42G=
XM_017009484.1:c.1959-42G= XP_016864973.1:n.1959-42G=
XM_017009485.1:c.1881-42G= XP_016864974.1:n.1881-42G=
XR_001742068.2:n.2401-42G=
NM_005921.2:c.2370-42G= MANE Select NP_005912.1:n.2370-42G=