Canonical Allele Identifier: CA2629083463
Gene: MAP2K1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66481982_66482000del , CM000677.2:g.66481982_66482000del GRCh38
NC_000015.9:g.66774320_66774338del , CM000677.1:g.66774320_66774338del GRCh37
NC_000015.8:g.64561374_64561392del NCBI36
NG_008305.1:g.100110_100128del , LRG_725:g.100110_100128del

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.627+103_627+121del ENSP00000508681.1:n.627+103_627+121del
ENST00000685172.1:c.693+103_693+121del ENSP00000509604.1:n.693+103_693+121del
ENST00000685763.1:c.546+103_546+121del ENSP00000509016.1:n.546+103_546+121del
ENST00000686347.1:c.569-5246_569-5228del ENSP00000509027.1:n.569-5246_569-5228del
ENST00000687191.1:n.1051+103_1051+121del
ENST00000689951.1:c.744+103_744+121del ENSP00000509308.1:n.744+103_744+121del
ENST00000691077.1:c.693+103_693+121del ENSP00000509843.1:n.693+103_693+121del
ENST00000691576.1:c.569-3012_569-2994del ENSP00000510066.1:n.569-3012_569-2994del
ENST00000691937.1:c.693+103_693+121del ENSP00000508768.1:n.693+103_693+121del
ENST00000692487.1:c.693+103_693+121del ENSP00000509534.1:n.693+103_693+121del
ENST00000692683.1:c.627+103_627+121del ENSP00000508437.1:n.627+103_627+121del
ENST00000693150.1:c.549+103_549+121del ENSP00000510309.1:n.549+103_549+121del
ENST00000307102.10:c.693+103_693+121del MANE Select ENSP00000302486.5:n.693+103_693+121del
ENST00000307102.9:c.693+103_693+121del ENSP00000302486.4:n.693+103_693+121del
ENST00000566326.1:c.165+103_165+121del ENSP00000456438.1:n.165+103_165+121del
NM_002755.3:c.693+103_693+121del , LRG_725t1:c.693+103_693+121del NP_002746.1:n.693+103_693+121del
XM_011521783.1:c.627+103_627+121del XP_011520085.1:n.627+103_627+121del
XM_011521783.3:c.627+103_627+121del XP_011520085.1:n.627+103_627+121del
XM_017022411.2:c.615+103_615+121del XP_016877900.1:n.615+103_615+121del
XM_017022412.1:c.549+103_549+121del XP_016877901.1:n.549+103_549+121del
XM_017022413.1:c.165+103_165+121del XP_016877902.1:n.165+103_165+121del
NM_002755.4:c.693+103_693+121del MANE Select NP_002746.1:n.693+103_693+121del