Canonical Allele Identifier: CA1548139531
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56882272G= , CM000667.2:g.56882272G= GRCh38
NC_000005.9:g.56178099G= , CM000667.1:g.56178099G= GRCh37
NC_000005.8:g.56213856G= NCBI36
NG_031884.1:g.72200G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.3072G= MANE Select ENSP00000382423.3:p.Lys1024=
ENST00000399503.3:c.3072G= ENSP00000382423.3:p.Lys1024=
NM_005921.1:c.3072G= NP_005912.1:p.Lys1024=
XM_005248519.3:c.2694G= XP_005248576.2:p.Lys898=
XM_011543406.1:c.2817G= XP_011541708.1:p.Lys939=
XM_011543407.1:c.2793G= XP_011541709.1:p.Lys931=
XM_011543408.1:c.3072G= XP_011541710.1:p.Lys1024=
XM_017009484.1:c.2661G= XP_016864973.1:p.Lys887=
XM_017009485.1:c.2583G= XP_016864974.1:p.Lys861=
XR_001742068.2:n.3103G=
NM_005921.2:c.3072G= MANE Select NP_005912.1:p.Lys1024=