Canonical Allele Identifier: CA2629083379
Gene: MAP2K1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66481699_66481703del , CM000677.2:g.66481699_66481703del GRCh38
NC_000015.9:g.66774037_66774041del , CM000677.1:g.66774037_66774041del GRCh37
NC_000015.8:g.64561091_64561095del NCBI36
NG_008305.1:g.99827_99831del , LRG_725:g.99827_99831del

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.503-56_503-52del ENSP00000508681.1:n.503-56_503-52del
ENST00000685172.1:c.569-56_569-52del ENSP00000509604.1:n.569-56_569-52del
ENST00000685763.1:c.422-56_422-52del ENSP00000509016.1:n.422-56_422-52del
ENST00000686347.1:c.569-5529_569-5525del ENSP00000509027.1:n.569-5529_569-5525del
ENST00000687191.1:n.927-56_927-52del
ENST00000689951.1:c.620-56_620-52del ENSP00000509308.1:n.620-56_620-52del
ENST00000691077.1:c.569-56_569-52del ENSP00000509843.1:n.569-56_569-52del
ENST00000691576.1:c.569-3295_569-3291del ENSP00000510066.1:n.569-3295_569-3291del
ENST00000691937.1:c.569-56_569-52del ENSP00000508768.1:n.569-56_569-52del
ENST00000692487.1:c.569-56_569-52del ENSP00000509534.1:n.569-56_569-52del
ENST00000692683.1:c.503-56_503-52del ENSP00000508437.1:n.503-56_503-52del
ENST00000693150.1:c.425-56_425-52del ENSP00000510309.1:n.425-56_425-52del
ENST00000307102.10:c.569-56_569-52del MANE Select ENSP00000302486.5:n.569-56_569-52del
ENST00000307102.9:c.569-56_569-52del ENSP00000302486.4:n.569-56_569-52del
ENST00000566326.1:c.41-56_41-52del ENSP00000456438.1:n.41-56_41-52del
NM_002755.3:c.569-56_569-52del , LRG_725t1:c.569-56_569-52del NP_002746.1:n.569-56_569-52del
XM_011521783.1:c.503-56_503-52del XP_011520085.1:n.503-56_503-52del
XM_011521783.3:c.503-56_503-52del XP_011520085.1:n.503-56_503-52del
XM_017022411.2:c.491-56_491-52del XP_016877900.1:n.491-56_491-52del
XM_017022412.1:c.425-56_425-52del XP_016877901.1:n.425-56_425-52del
XM_017022413.1:c.41-56_41-52del XP_016877902.1:n.41-56_41-52del
NM_002755.4:c.569-56_569-52del MANE Select NP_002746.1:n.569-56_569-52del