Canonical Allele Identifier: CA392937260
Gene: MAP2K1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.66777443A>C (hg19) chr15:g.66485105A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66485105A>C , CM000677.2:g.66485105A>C GRCh38
NC_000015.9:g.66777443A>C , CM000677.1:g.66777443A>C GRCh37
NC_000015.8:g.64564497A>C NCBI36
NG_008305.1:g.103233A>C , LRG_725:g.103233A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.628-2123A>C ENSP00000508681.1:n.628-2123A>C
ENST00000685172.1:c.809A>C ENSP00000509604.1:p.Glu270Ala
ENST00000685763.1:c.662A>C ENSP00000509016.1:p.Glu221Ala
ENST00000686347.1:c.569-2123A>C ENSP00000509027.1:n.569-2123A>C
ENST00000687191.1:n.1167A>C
ENST00000687481.1:n.224A>C
ENST00000689951.1:c.860A>C ENSP00000509308.1:p.Glu287Ala
ENST00000691077.1:c.*46A>C ENSP00000509843.1:n.*46A>C
ENST00000691576.1:c.680A>C ENSP00000510066.1:p.Glu227Ala
ENST00000691937.1:c.809A>C ENSP00000508768.1:p.Glu270Ala
ENST00000692487.1:c.*46A>C ENSP00000509534.1:n.*46A>C
ENST00000692683.1:c.743A>C ENSP00000508437.1:p.Glu248Ala
ENST00000693150.1:c.665A>C ENSP00000510309.1:p.Glu222Ala
ENST00000307102.10:c.809A>C MANE Select ENSP00000302486.5:p.Glu270Ala
ENST00000307102.9:c.809A>C ENSP00000302486.4:p.Glu270Ala
ENST00000566326.1:c.281A>C ENSP00000456438.1:p.Glu94Ala
NM_002755.3:c.809A>C , LRG_725t1:c.809A>C NP_002746.1:p.Glu270Ala
XM_011521783.1:c.743A>C XP_011520085.1:p.Glu248Ala
XM_011521783.3:c.743A>C XP_011520085.1:p.Glu248Ala
XM_017022411.2:c.731A>C XP_016877900.1:p.Glu244Ala
XM_017022412.1:c.665A>C XP_016877901.1:p.Glu222Ala
XM_017022413.1:c.281A>C XP_016877902.1:p.Glu94Ala
NM_002755.4:c.809A>C MANE Select NP_002746.1:p.Glu270Ala
Search 100 bp 5'
Search 100 bp 3'