Canonical Allele Identifier: CA1548139507
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56882223G= , CM000667.2:g.56882223G= GRCh38
NC_000005.9:g.56178050G= , CM000667.1:g.56178050G= GRCh37
NC_000005.8:g.56213807G= NCBI36
NG_031884.1:g.72151G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.3023G= MANE Select ENSP00000382423.3:p.Gly1008=
ENST00000399503.3:c.3023G= ENSP00000382423.3:p.Gly1008=
NM_005921.1:c.3023G= NP_005912.1:p.Gly1008=
XM_005248519.3:c.2645G= XP_005248576.2:p.Gly882=
XM_011543406.1:c.2768G= XP_011541708.1:p.Gly923=
XM_011543407.1:c.2744G= XP_011541709.1:p.Gly915=
XM_011543408.1:c.3023G= XP_011541710.1:p.Gly1008=
XM_017009484.1:c.2612G= XP_016864973.1:p.Gly871=
XM_017009485.1:c.2534G= XP_016864974.1:p.Gly845=
XR_001742068.2:n.3054G=
NM_005921.2:c.3023G= MANE Select NP_005912.1:p.Gly1008=