Canonical Allele Identifier: CA2184099974
Gene: MAP2K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66484985T= , CM000677.2:g.66484985T= GRCh38
NC_000015.9:g.66777323T= , CM000677.1:g.66777323T= GRCh37
NC_000015.8:g.64564377T= NCBI36
NG_008305.1:g.103113T= , LRG_725:g.103113T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.628-2243T= ENSP00000508681.1:n.628-2243T=
ENST00000685172.1:c.694-5T= ENSP00000509604.1:n.694-5T=
ENST00000685763.1:c.547-5T= ENSP00000509016.1:n.547-5T=
ENST00000686347.1:c.569-2243T= ENSP00000509027.1:n.569-2243T=
ENST00000687191.1:n.1052-5T=
ENST00000687481.1:n.104T=
ENST00000689951.1:c.745-5T= ENSP00000509308.1:n.745-5T=
ENST00000691077.1:c.694-9T= ENSP00000509843.1:n.694-9T=
ENST00000691576.1:c.569-9T= ENSP00000510066.1:n.569-9T=
ENST00000691937.1:c.694-5T= ENSP00000508768.1:n.694-5T=
ENST00000692487.1:c.694-9T= ENSP00000509534.1:n.694-9T=
ENST00000692683.1:c.628-5T= ENSP00000508437.1:n.628-5T=
ENST00000693150.1:c.550-5T= ENSP00000510309.1:n.550-5T=
ENST00000307102.10:c.694-5T= MANE Select ENSP00000302486.5:n.694-5T=
ENST00000307102.9:c.694-5T= ENSP00000302486.4:n.694-5T=
ENST00000566326.1:c.166-5T= ENSP00000456438.1:n.166-5T=
NM_002755.3:c.694-5T= , LRG_725t1:c.694-5T= NP_002746.1:n.694-5T=
XM_011521783.1:c.628-5T= XP_011520085.1:n.628-5T=
XM_011521783.3:c.628-5T= XP_011520085.1:n.628-5T=
XM_017022411.2:c.616-5T= XP_016877900.1:n.616-5T=
XM_017022412.1:c.550-5T= XP_016877901.1:n.550-5T=
XM_017022413.1:c.166-5T= XP_016877902.1:n.166-5T=
NM_002755.4:c.694-5T= MANE Select NP_002746.1:n.694-5T=