Canonical Allele Identifier: CA2184100110
Gene: MAP2K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66485149G= , CM000677.2:g.66485149G= GRCh38
NC_000015.9:g.66777487G= , CM000677.1:g.66777487G= GRCh37
NC_000015.8:g.64564541G= NCBI36
NG_008305.1:g.103277G= , LRG_725:g.103277G=

Transcript Alleles

HGVS Amino-acid change
ENST00000684779.1:c.628-2079G= ENSP00000508681.1:n.628-2079G=
ENST00000685172.1:c.853G= ENSP00000509604.1:p.Glu285=
ENST00000685763.1:c.706G= ENSP00000509016.1:p.Glu236=
ENST00000686347.1:c.569-2079G= ENSP00000509027.1:n.569-2079G=
ENST00000687191.1:n.1211G=
ENST00000687481.1:n.268G=
ENST00000689951.1:c.904G= ENSP00000509308.1:p.Glu302=
ENST00000691077.1:c.*90G= ENSP00000509843.1:n.*90G=
ENST00000691576.1:c.724G= ENSP00000510066.1:p.Glu242=
ENST00000691937.1:c.853G= ENSP00000508768.1:p.Glu285=
ENST00000692487.1:c.*90G= ENSP00000509534.1:n.*90G=
ENST00000692683.1:c.787G= ENSP00000508437.1:p.Glu263=
ENST00000693150.1:c.709G= ENSP00000510309.1:p.Glu237=
ENST00000307102.10:c.853G= MANE Select ENSP00000302486.5:p.Glu285=
ENST00000307102.9:c.853G= ENSP00000302486.4:p.Glu285=
ENST00000566326.1:c.325G= ENSP00000456438.1:p.Glu109=
NM_002755.3:c.853G= , LRG_725t1:c.853G= NP_002746.1:p.Glu285=
XM_011521783.1:c.787G= XP_011520085.1:p.Glu263=
XM_011521783.3:c.787G= XP_011520085.1:p.Glu263=
XM_017022411.2:c.775G= XP_016877900.1:p.Glu259=
XM_017022412.1:c.709G= XP_016877901.1:p.Glu237=
XM_017022413.1:c.325G= XP_016877902.1:p.Glu109=
NM_002755.4:c.853G= MANE Select NP_002746.1:p.Glu285=