Canonical Allele Identifier: CA2629083384
Gene: MAP2K1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66481698_66481700dup , CM000677.2:g.66481698_66481700dup GRCh38
NC_000015.9:g.66774036_66774038dup , CM000677.1:g.66774036_66774038dup GRCh37
NC_000015.8:g.64561090_64561092dup NCBI36
NG_008305.1:g.99826_99828dup , LRG_725:g.99826_99828dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.503-57_503-55dup ENSP00000508681.1:n.503-57_503-55dup
ENST00000685172.1:c.569-57_569-55dup ENSP00000509604.1:n.569-57_569-55dup
ENST00000685763.1:c.422-57_422-55dup ENSP00000509016.1:n.422-57_422-55dup
ENST00000686347.1:c.569-5530_569-5528dup ENSP00000509027.1:n.569-5530_569-5528dup
ENST00000687191.1:n.927-57_927-55dup
ENST00000689951.1:c.620-57_620-55dup ENSP00000509308.1:n.620-57_620-55dup
ENST00000691077.1:c.569-57_569-55dup ENSP00000509843.1:n.569-57_569-55dup
ENST00000691576.1:c.569-3296_569-3294dup ENSP00000510066.1:n.569-3296_569-3294dup
ENST00000691937.1:c.569-57_569-55dup ENSP00000508768.1:n.569-57_569-55dup
ENST00000692487.1:c.569-57_569-55dup ENSP00000509534.1:n.569-57_569-55dup
ENST00000692683.1:c.503-57_503-55dup ENSP00000508437.1:n.503-57_503-55dup
ENST00000693150.1:c.425-57_425-55dup ENSP00000510309.1:n.425-57_425-55dup
ENST00000307102.10:c.569-57_569-55dup MANE Select ENSP00000302486.5:n.569-57_569-55dup
ENST00000307102.9:c.569-57_569-55dup ENSP00000302486.4:n.569-57_569-55dup
ENST00000566326.1:c.41-57_41-55dup ENSP00000456438.1:n.41-57_41-55dup
NM_002755.3:c.569-57_569-55dup , LRG_725t1:c.569-57_569-55dup NP_002746.1:n.569-57_569-55dup
XM_011521783.1:c.503-57_503-55dup XP_011520085.1:n.503-57_503-55dup
XM_011521783.3:c.503-57_503-55dup XP_011520085.1:n.503-57_503-55dup
XM_017022411.2:c.491-57_491-55dup XP_016877900.1:n.491-57_491-55dup
XM_017022412.1:c.425-57_425-55dup XP_016877901.1:n.425-57_425-55dup
XM_017022413.1:c.41-57_41-55dup XP_016877902.1:n.41-57_41-55dup
NM_002755.4:c.569-57_569-55dup MANE Select NP_002746.1:n.569-57_569-55dup