Canonical Allele Identifier: CA2629083589
Gene: MAP2K1 HGNC NCBI

Linked Data

dbSNP Id: rs2140673570

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66484975C>T , CM000677.2:g.66484975C>T GRCh38
NC_000015.9:g.66777313C>T , CM000677.1:g.66777313C>T GRCh37
NC_000015.8:g.64564367C>T NCBI36
NG_008305.1:g.103103C>T , LRG_725:g.103103C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000684779.1:c.628-2253C>T ENSP00000508681.1:n.628-2253C>T
ENST00000685172.1:c.694-15C>T ENSP00000509604.1:n.694-15C>T
ENST00000685763.1:c.547-15C>T ENSP00000509016.1:n.547-15C>T
ENST00000686347.1:c.569-2253C>T ENSP00000509027.1:n.569-2253C>T
ENST00000687191.1:n.1052-15C>T
ENST00000687481.1:n.94C>T
ENST00000689951.1:c.745-15C>T ENSP00000509308.1:n.745-15C>T
ENST00000691077.1:c.694-19C>T ENSP00000509843.1:n.694-19C>T
ENST00000691576.1:c.569-19C>T ENSP00000510066.1:n.569-19C>T
ENST00000691937.1:c.694-15C>T ENSP00000508768.1:n.694-15C>T
ENST00000692487.1:c.694-19C>T ENSP00000509534.1:n.694-19C>T
ENST00000692683.1:c.628-15C>T ENSP00000508437.1:n.628-15C>T
ENST00000693150.1:c.550-15C>T ENSP00000510309.1:n.550-15C>T
ENST00000307102.10:c.694-15C>T MANE Select ENSP00000302486.5:n.694-15C>T
ENST00000307102.9:c.694-15C>T ENSP00000302486.4:n.694-15C>T
ENST00000566326.1:c.166-15C>T ENSP00000456438.1:n.166-15C>T
NM_002755.3:c.694-15C>T , LRG_725t1:c.694-15C>T NP_002746.1:n.694-15C>T
XM_011521783.1:c.628-15C>T XP_011520085.1:n.628-15C>T
XM_011521783.3:c.628-15C>T XP_011520085.1:n.628-15C>T
XM_017022411.2:c.616-15C>T XP_016877900.1:n.616-15C>T
XM_017022412.1:c.550-15C>T XP_016877901.1:n.550-15C>T
XM_017022413.1:c.166-15C>T XP_016877902.1:n.166-15C>T
NM_002755.4:c.694-15C>T MANE Select NP_002746.1:n.694-15C>T