Canonical Allele Identifier: CA2184100081
Gene: MAP2K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66485129A= , CM000677.2:g.66485129A= GRCh38
NC_000015.9:g.66777467A= , CM000677.1:g.66777467A= GRCh37
NC_000015.8:g.64564521A= NCBI36
NG_008305.1:g.103257A= , LRG_725:g.103257A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.628-2099A= ENSP00000508681.1:n.628-2099A=
ENST00000685172.1:c.833A= ENSP00000509604.1:p.Gln278=
ENST00000685763.1:c.686A= ENSP00000509016.1:p.Gln229=
ENST00000686347.1:c.569-2099A= ENSP00000509027.1:n.569-2099A=
ENST00000687191.1:n.1191A=
ENST00000687481.1:n.248A=
ENST00000689951.1:c.884A= ENSP00000509308.1:p.Gln295=
ENST00000691077.1:c.*70A= ENSP00000509843.1:n.*70A=
ENST00000691576.1:c.704A= ENSP00000510066.1:p.Gln235=
ENST00000691937.1:c.833A= ENSP00000508768.1:p.Gln278=
ENST00000692487.1:c.*70A= ENSP00000509534.1:n.*70A=
ENST00000692683.1:c.767A= ENSP00000508437.1:p.Gln256=
ENST00000693150.1:c.689A= ENSP00000510309.1:p.Gln230=
ENST00000307102.10:c.833A= MANE Select ENSP00000302486.5:p.Gln278=
ENST00000307102.9:c.833A= ENSP00000302486.4:p.Gln278=
ENST00000566326.1:c.305A= ENSP00000456438.1:p.Gln102=
NM_002755.3:c.833A= , LRG_725t1:c.833A= NP_002746.1:p.Gln278=
XM_011521783.1:c.767A= XP_011520085.1:p.Gln256=
XM_011521783.3:c.767A= XP_011520085.1:p.Gln256=
XM_017022411.2:c.755A= XP_016877900.1:p.Gln252=
XM_017022412.1:c.689A= XP_016877901.1:p.Gln230=
XM_017022413.1:c.305A= XP_016877902.1:p.Gln102=
NM_002755.4:c.833A= MANE Select NP_002746.1:p.Gln278=