Canonical Allele Identifier: CA2184097405
Gene: MAP2K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66481789T= , CM000677.2:g.66481789T= GRCh38
NC_000015.9:g.66774127T= , CM000677.1:g.66774127T= GRCh37
NC_000015.8:g.64561181T= NCBI36
NG_008305.1:g.99917T= , LRG_725:g.99917T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.537T= ENSP00000508681.1:p.Arg179=
ENST00000685172.1:c.603T= ENSP00000509604.1:p.Arg201=
ENST00000685763.1:c.456T= ENSP00000509016.1:p.Arg152=
ENST00000686347.1:c.569-5439T= ENSP00000509027.1:n.569-5439T=
ENST00000687191.1:n.961T=
ENST00000689951.1:c.654T= ENSP00000509308.1:p.Arg218=
ENST00000691077.1:c.603T= ENSP00000509843.1:p.Arg201=
ENST00000691576.1:c.569-3205T= ENSP00000510066.1:n.569-3205T=
ENST00000691937.1:c.603T= ENSP00000508768.1:p.Arg201=
ENST00000692487.1:c.603T= ENSP00000509534.1:p.Arg201=
ENST00000692683.1:c.537T= ENSP00000508437.1:p.Arg179=
ENST00000693150.1:c.459T= ENSP00000510309.1:p.Arg153=
ENST00000307102.10:c.603T= MANE Select ENSP00000302486.5:p.Arg201=
ENST00000307102.9:c.603T= ENSP00000302486.4:p.Arg201=
ENST00000566326.1:c.75T= ENSP00000456438.1:p.Arg25=
NM_002755.3:c.603T= , LRG_725t1:c.603T= NP_002746.1:p.Arg201=
XM_011521783.1:c.537T= XP_011520085.1:p.Arg179=
XM_011521783.3:c.537T= XP_011520085.1:p.Arg179=
XM_017022411.2:c.525T= XP_016877900.1:p.Arg175=
XM_017022412.1:c.459T= XP_016877901.1:p.Arg153=
XM_017022413.1:c.75T= XP_016877902.1:p.Arg25=
NM_002755.4:c.603T= MANE Select NP_002746.1:p.Arg201=