Canonical Allele Identifier: CA618679482
Gene: MAP2K1 HGNC NCBI

Linked Data

dbSNP Id: rs1478790848

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66481504_66481505del , CM000677.2:g.66481504_66481505del GRCh38
NC_000015.9:g.66773842_66773843del , CM000677.1:g.66773842_66773843del GRCh37
NC_000015.8:g.64560896_64560897del NCBI36
NG_008305.1:g.99632_99633del , LRG_725:g.99632_99633del

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.503-251_503-250del ENSP00000508681.1:n.503-251_503-250del
ENST00000685172.1:c.569-251_569-250del ENSP00000509604.1:n.569-251_569-250del
ENST00000685763.1:c.422-251_422-250del ENSP00000509016.1:n.422-251_422-250del
ENST00000686347.1:c.569-5724_569-5723del ENSP00000509027.1:n.569-5724_569-5723del
ENST00000687191.1:n.927-251_927-250del
ENST00000689951.1:c.620-251_620-250del ENSP00000509308.1:n.620-251_620-250del
ENST00000691077.1:c.569-251_569-250del ENSP00000509843.1:n.569-251_569-250del
ENST00000691576.1:c.569-3490_569-3489del ENSP00000510066.1:n.569-3490_569-3489del
ENST00000691937.1:c.569-251_569-250del ENSP00000508768.1:n.569-251_569-250del
ENST00000692487.1:c.569-251_569-250del ENSP00000509534.1:n.569-251_569-250del
ENST00000692683.1:c.503-251_503-250del ENSP00000508437.1:n.503-251_503-250del
ENST00000693150.1:c.425-251_425-250del ENSP00000510309.1:n.425-251_425-250del
ENST00000307102.10:c.569-251_569-250del MANE Select ENSP00000302486.5:n.569-251_569-250del
ENST00000307102.9:c.569-251_569-250del ENSP00000302486.4:n.569-251_569-250del
ENST00000566326.1:c.41-251_41-250del ENSP00000456438.1:n.41-251_41-250del
NM_002755.3:c.569-251_569-250del , LRG_725t1:c.569-251_569-250del NP_002746.1:n.569-251_569-250del
XM_011521783.1:c.503-251_503-250del XP_011520085.1:n.503-251_503-250del
XM_011521783.3:c.503-251_503-250del XP_011520085.1:n.503-251_503-250del
XM_017022411.2:c.491-251_491-250del XP_016877900.1:n.491-251_491-250del
XM_017022412.1:c.425-251_425-250del XP_016877901.1:n.425-251_425-250del
XM_017022413.1:c.41-251_41-250del XP_016877902.1:n.41-251_41-250del
NM_002755.4:c.569-251_569-250del MANE Select NP_002746.1:n.569-251_569-250del