Canonical Allele Identifier: CA2184097510
Gene: MAP2K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66481932_66481933delinsGC , CM000677.2:g.66481932_66481933delinsGC GRCh38
NC_000015.9:g.66774270_66774271delinsGC , CM000677.1:g.66774270_66774271delinsGC GRCh37
NC_000015.8:g.64561324_64561325delinsGC NCBI36
NG_008305.1:g.100060_100061delinsGC , LRG_725:g.100060_100061delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.627+53_627+54delinsGC ENSP00000508681.1:n.627+53_627+54delinsGC
ENST00000685172.1:c.693+53_693+54delinsGC ENSP00000509604.1:n.693+53_693+54delinsGC
ENST00000685763.1:c.546+53_546+54delinsGC ENSP00000509016.1:n.546+53_546+54delinsGC
ENST00000686347.1:c.569-5296_569-5295delinsGC ENSP00000509027.1:n.569-5296_569-5295delinsGC
ENST00000687191.1:n.1051+53_1051+54delinsGC
ENST00000689951.1:c.744+53_744+54delinsGC ENSP00000509308.1:n.744+53_744+54delinsGC
ENST00000691077.1:c.693+53_693+54delinsGC ENSP00000509843.1:n.693+53_693+54delinsGC
ENST00000691576.1:c.569-3062_569-3061delinsGC ENSP00000510066.1:n.569-3062_569-3061delinsGC
ENST00000691937.1:c.693+53_693+54delinsGC ENSP00000508768.1:n.693+53_693+54delinsGC
ENST00000692487.1:c.693+53_693+54delinsGC ENSP00000509534.1:n.693+53_693+54delinsGC
ENST00000692683.1:c.627+53_627+54delinsGC ENSP00000508437.1:n.627+53_627+54delinsGC
ENST00000693150.1:c.549+53_549+54delinsGC ENSP00000510309.1:n.549+53_549+54delinsGC
ENST00000307102.10:c.693+53_693+54delinsGC MANE Select ENSP00000302486.5:n.693+53_693+54delinsGC
ENST00000307102.9:c.693+53_693+54delinsGC ENSP00000302486.4:n.693+53_693+54delinsGC
ENST00000566326.1:c.165+53_165+54delinsGC ENSP00000456438.1:n.165+53_165+54delinsGC
NM_002755.3:c.693+53_693+54delinsGC , LRG_725t1:c.693+53_693+54delinsGC NP_002746.1:n.693+53_693+54delinsGC
XM_011521783.1:c.627+53_627+54delinsGC XP_011520085.1:n.627+53_627+54delinsGC
XM_011521783.3:c.627+53_627+54delinsGC XP_011520085.1:n.627+53_627+54delinsGC
XM_017022411.2:c.615+53_615+54delinsGC XP_016877900.1:n.615+53_615+54delinsGC
XM_017022412.1:c.549+53_549+54delinsGC XP_016877901.1:n.549+53_549+54delinsGC
XM_017022413.1:c.165+53_165+54delinsGC XP_016877902.1:n.165+53_165+54delinsGC
NM_002755.4:c.693+53_693+54delinsGC MANE Select NP_002746.1:n.693+53_693+54delinsGC