Canonical Allele Identifier: CA1548139574
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56882383G= , CM000667.2:g.56882383G= GRCh38
NC_000005.9:g.56178210G= , CM000667.1:g.56178210G= GRCh37
NC_000005.8:g.56213967G= NCBI36
NG_031884.1:g.72311G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.3183G= MANE Select ENSP00000382423.3:p.Lys1061=
ENST00000399503.3:c.3183G= ENSP00000382423.3:p.Lys1061=
NM_005921.1:c.3183G= NP_005912.1:p.Lys1061=
XM_005248519.3:c.2805G= XP_005248576.2:p.Lys935=
XM_011543406.1:c.2928G= XP_011541708.1:p.Lys976=
XM_011543407.1:c.2904G= XP_011541709.1:p.Lys968=
XM_011543408.1:c.3183G= XP_011541710.1:p.Lys1061=
XM_017009484.1:c.2772G= XP_016864973.1:p.Lys924=
XM_017009485.1:c.2694G= XP_016864974.1:p.Lys898=
XR_001742068.2:n.3214G=
NM_005921.2:c.3183G= MANE Select NP_005912.1:p.Lys1061=