Canonical Allele Identifier: CA2184071749
Gene: MAP2K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66435120G= , CM000677.2:g.66435120G= GRCh38
NC_000015.9:g.66727458G= , CM000677.1:g.66727458G= GRCh37
NC_000015.8:g.64514512G= NCBI36
NG_008305.1:g.53248G= , LRG_725:g.53248G=

Transcript Alleles

HGVS Amino-acid change
ENST00000684779.1:c.108G= ENSP00000508681.1:p.Gln36=
ENST00000685172.1:c.174G= ENSP00000509604.1:p.Gln58=
ENST00000685763.1:c.174G= ENSP00000509016.1:p.Gln58=
ENST00000686347.1:c.174G= ENSP00000509027.1:p.Gln58=
ENST00000687191.1:n.610G=
ENST00000689951.1:c.174G= ENSP00000509308.1:p.Gln58=
ENST00000691077.1:c.174G= ENSP00000509843.1:p.Gln58=
ENST00000691576.1:c.174G= ENSP00000510066.1:p.Gln58=
ENST00000691937.1:c.174G= ENSP00000508768.1:p.Gln58=
ENST00000692487.1:c.174G= ENSP00000509534.1:p.Gln58=
ENST00000692683.1:c.108G= ENSP00000508437.1:p.Gln36=
ENST00000693150.1:c.108G= ENSP00000510309.1:p.Gln36=
ENST00000307102.10:c.174G= MANE Select ENSP00000302486.5:p.Gln58=
ENST00000307102.9:c.174G= ENSP00000302486.4:p.Gln58=
ENST00000425818.2:n.685G=
NM_002755.3:c.174G= , LRG_725t1:c.174G= NP_002746.1:p.Gln58=
XM_011521783.1:c.108G= XP_011520085.1:p.Gln36=
XM_011521783.3:c.108G= XP_011520085.1:p.Gln36=
XM_017022411.2:c.174G= XP_016877900.1:p.Gln58=
XM_017022412.1:c.108G= XP_016877901.1:p.Gln36=
NM_002755.4:c.174G= MANE Select NP_002746.1:p.Gln58=