Canonical Allele Identifier: CA2184097461
Gene: MAP2K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66481855C= , CM000677.2:g.66481855C= GRCh38
NC_000015.9:g.66774193C= , CM000677.1:g.66774193C= GRCh37
NC_000015.8:g.64561247C= NCBI36
NG_008305.1:g.99983C= , LRG_725:g.99983C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.603C= ENSP00000508681.1:p.Phe201=
ENST00000685172.1:c.669C= ENSP00000509604.1:p.Phe223=
ENST00000685763.1:c.522C= ENSP00000509016.1:p.Phe174=
ENST00000686347.1:c.569-5373C= ENSP00000509027.1:n.569-5373C=
ENST00000687191.1:n.1027C=
ENST00000689951.1:c.720C= ENSP00000509308.1:p.Phe240=
ENST00000691077.1:c.669C= ENSP00000509843.1:p.Phe223=
ENST00000691576.1:c.569-3139C= ENSP00000510066.1:n.569-3139C=
ENST00000691937.1:c.669C= ENSP00000508768.1:p.Phe223=
ENST00000692487.1:c.669C= ENSP00000509534.1:p.Phe223=
ENST00000692683.1:c.603C= ENSP00000508437.1:p.Phe201=
ENST00000693150.1:c.525C= ENSP00000510309.1:p.Phe175=
ENST00000307102.10:c.669C= MANE Select ENSP00000302486.5:p.Phe223=
ENST00000307102.9:c.669C= ENSP00000302486.4:p.Phe223=
ENST00000566326.1:c.141C= ENSP00000456438.1:p.Phe47=
NM_002755.3:c.669C= , LRG_725t1:c.669C= NP_002746.1:p.Phe223=
XM_011521783.1:c.603C= XP_011520085.1:p.Phe201=
XM_011521783.3:c.603C= XP_011520085.1:p.Phe201=
XM_017022411.2:c.591C= XP_016877900.1:p.Phe197=
XM_017022412.1:c.525C= XP_016877901.1:p.Phe175=
XM_017022413.1:c.141C= XP_016877902.1:p.Phe47=
NM_002755.4:c.669C= MANE Select NP_002746.1:p.Phe223=