Canonical Allele Identifier: CA2629083397
Gene: MAP2K1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66481720_66481721del , CM000677.2:g.66481720_66481721del GRCh38
NC_000015.9:g.66774058_66774059del , CM000677.1:g.66774058_66774059del GRCh37
NC_000015.8:g.64561112_64561113del NCBI36
NG_008305.1:g.99848_99849del , LRG_725:g.99848_99849del

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.503-35_503-34del ENSP00000508681.1:n.503-35_503-34del
ENST00000685172.1:c.569-35_569-34del ENSP00000509604.1:n.569-35_569-34del
ENST00000685763.1:c.422-35_422-34del ENSP00000509016.1:n.422-35_422-34del
ENST00000686347.1:c.569-5508_569-5507del ENSP00000509027.1:n.569-5508_569-5507del
ENST00000687191.1:n.927-35_927-34del
ENST00000689951.1:c.620-35_620-34del ENSP00000509308.1:n.620-35_620-34del
ENST00000691077.1:c.569-35_569-34del ENSP00000509843.1:n.569-35_569-34del
ENST00000691576.1:c.569-3274_569-3273del ENSP00000510066.1:n.569-3274_569-3273del
ENST00000691937.1:c.569-35_569-34del ENSP00000508768.1:n.569-35_569-34del
ENST00000692487.1:c.569-35_569-34del ENSP00000509534.1:n.569-35_569-34del
ENST00000692683.1:c.503-35_503-34del ENSP00000508437.1:n.503-35_503-34del
ENST00000693150.1:c.425-35_425-34del ENSP00000510309.1:n.425-35_425-34del
ENST00000307102.10:c.569-35_569-34del MANE Select ENSP00000302486.5:n.569-35_569-34del
ENST00000307102.9:c.569-35_569-34del ENSP00000302486.4:n.569-35_569-34del
ENST00000566326.1:c.41-35_41-34del ENSP00000456438.1:n.41-35_41-34del
NM_002755.3:c.569-35_569-34del , LRG_725t1:c.569-35_569-34del NP_002746.1:n.569-35_569-34del
XM_011521783.1:c.503-35_503-34del XP_011520085.1:n.503-35_503-34del
XM_011521783.3:c.503-35_503-34del XP_011520085.1:n.503-35_503-34del
XM_017022411.2:c.491-35_491-34del XP_016877900.1:n.491-35_491-34del
XM_017022412.1:c.425-35_425-34del XP_016877901.1:n.425-35_425-34del
XM_017022413.1:c.41-35_41-34del XP_016877902.1:n.41-35_41-34del
NM_002755.4:c.569-35_569-34del MANE Select NP_002746.1:n.569-35_569-34del