Canonical Allele Identifier: CA1548139277
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56881734G= , CM000667.2:g.56881734G= GRCh38
NC_000005.9:g.56177561G= , CM000667.1:g.56177561G= GRCh37
NC_000005.8:g.56213318G= NCBI36
NG_031884.1:g.71662G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.2534G= MANE Select ENSP00000382423.3:p.Ser845=
ENST00000399503.3:c.2534G= ENSP00000382423.3:p.Ser845=
NM_005921.1:c.2534G= NP_005912.1:p.Ser845=
XM_005248519.3:c.2156G= XP_005248576.2:p.Ser719=
XM_011543406.1:c.2279G= XP_011541708.1:p.Ser760=
XM_011543407.1:c.2255G= XP_011541709.1:p.Ser752=
XM_011543408.1:c.2534G= XP_011541710.1:p.Ser845=
XM_017009484.1:c.2123G= XP_016864973.1:p.Ser708=
XM_017009485.1:c.2045G= XP_016864974.1:p.Ser682=
XR_001742068.2:n.2565G=
NM_005921.2:c.2534G= MANE Select NP_005912.1:p.Ser845=