Canonical Allele Identifier: CA2184097465
Gene: MAP2K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66481878C= , CM000677.2:g.66481878C= GRCh38
NC_000015.9:g.66774216C= , CM000677.1:g.66774216C= GRCh37
NC_000015.8:g.64561270C= NCBI36
NG_008305.1:g.100006C= , LRG_725:g.100006C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.626C= ENSP00000508681.1:p.Ser209=
ENST00000685172.1:c.692C= ENSP00000509604.1:p.Ser231=
ENST00000685763.1:c.545C= ENSP00000509016.1:p.Ser182=
ENST00000686347.1:c.569-5350C= ENSP00000509027.1:n.569-5350C=
ENST00000687191.1:n.1050C=
ENST00000689951.1:c.743C= ENSP00000509308.1:p.Ser248=
ENST00000691077.1:c.692C= ENSP00000509843.1:p.Ser231=
ENST00000691576.1:c.569-3116C= ENSP00000510066.1:n.569-3116C=
ENST00000691937.1:c.692C= ENSP00000508768.1:p.Ser231=
ENST00000692487.1:c.692C= ENSP00000509534.1:p.Ser231=
ENST00000692683.1:c.626C= ENSP00000508437.1:p.Ser209=
ENST00000693150.1:c.548C= ENSP00000510309.1:p.Ser183=
ENST00000307102.10:c.692C= MANE Select ENSP00000302486.5:p.Ser231=
ENST00000307102.9:c.692C= ENSP00000302486.4:p.Ser231=
ENST00000566326.1:c.164C= ENSP00000456438.1:p.Ser55=
NM_002755.3:c.692C= , LRG_725t1:c.692C= NP_002746.1:p.Ser231=
XM_011521783.1:c.626C= XP_011520085.1:p.Ser209=
XM_011521783.3:c.626C= XP_011520085.1:p.Ser209=
XM_017022411.2:c.614C= XP_016877900.1:p.Ser205=
XM_017022412.1:c.548C= XP_016877901.1:p.Ser183=
XM_017022413.1:c.164C= XP_016877902.1:p.Ser55=
NM_002755.4:c.692C= MANE Select NP_002746.1:p.Ser231=