Canonical Allele Identifier: CA1548129251
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56859871T= , CM000667.2:g.56859871T= GRCh38
NC_000005.9:g.56155698T= , CM000667.1:g.56155698T= GRCh37
NC_000005.8:g.56191455T= NCBI36
NG_031884.1:g.49799T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.790T= MANE Select ENSP00000382423.3:p.Ser264=
ENST00000399503.3:c.790T= ENSP00000382423.3:p.Ser264=
NM_005921.1:c.790T= NP_005912.1:p.Ser264=
XM_005248519.3:c.412T= XP_005248576.2:p.Ser138=
XM_011543406.1:c.535T= XP_011541708.1:p.Ser179=
XM_011543407.1:c.790T= XP_011541709.1:p.Ser264=
XM_011543408.1:c.790T= XP_011541710.1:p.Ser264=
XM_017009484.1:c.379T= XP_016864973.1:p.Ser127=
XM_017009485.1:c.301T= XP_016864974.1:p.Ser101=
XR_001742068.2:n.821T=
NM_005921.2:c.790T= MANE Select NP_005912.1:p.Ser264=