Canonical Allele Identifier: CA392937346
Gene: MAP2K1 HGNC NCBI

Linked Data

dbSNP Id: rs2140675186

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66485142T>A , CM000677.2:g.66485142T>A GRCh38
NC_000015.9:g.66777480T>A , CM000677.1:g.66777480T>A GRCh37
NC_000015.8:g.64564534T>A NCBI36
NG_008305.1:g.103270T>A , LRG_725:g.103270T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.628-2086T>A ENSP00000508681.1:n.628-2086T>A
ENST00000685172.1:c.846T>A ENSP00000509604.1:p.Asp282Glu
ENST00000685763.1:c.699T>A ENSP00000509016.1:p.Asp233Glu
ENST00000686347.1:c.569-2086T>A ENSP00000509027.1:n.569-2086T>A
ENST00000687191.1:n.1204T>A
ENST00000687481.1:n.261T>A
ENST00000689951.1:c.897T>A ENSP00000509308.1:p.Asp299Glu
ENST00000691077.1:c.*83T>A ENSP00000509843.1:n.*83T>A
ENST00000691576.1:c.717T>A ENSP00000510066.1:p.Asp239Glu
ENST00000691937.1:c.846T>A ENSP00000508768.1:p.Asp282Glu
ENST00000692487.1:c.*83T>A ENSP00000509534.1:n.*83T>A
ENST00000692683.1:c.780T>A ENSP00000508437.1:p.Asp260Glu
ENST00000693150.1:c.702T>A ENSP00000510309.1:p.Asp234Glu
ENST00000307102.10:c.846T>A MANE Select ENSP00000302486.5:p.Asp282Glu
ENST00000307102.9:c.846T>A ENSP00000302486.4:p.Asp282Glu
ENST00000566326.1:c.318T>A ENSP00000456438.1:p.Asp106Glu
NM_002755.3:c.846T>A , LRG_725t1:c.846T>A NP_002746.1:p.Asp282Glu
XM_011521783.1:c.780T>A XP_011520085.1:p.Asp260Glu
XM_011521783.3:c.780T>A XP_011520085.1:p.Asp260Glu
XM_017022411.2:c.768T>A XP_016877900.1:p.Asp256Glu
XM_017022412.1:c.702T>A XP_016877901.1:p.Asp234Glu
XM_017022413.1:c.318T>A XP_016877902.1:p.Asp106Glu
NM_002755.4:c.846T>A MANE Select NP_002746.1:p.Asp282Glu