Canonical Allele Identifier: CA645570539
Gene: MAP2K1 HGNC NCBI

Linked Data

COSMIC: COSM5702510
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66435128_66435142del , CM000677.2:g.66435128_66435142del GRCh38
NC_000015.9:g.66727466_66727480del , CM000677.1:g.66727466_66727480del GRCh37
NC_000015.8:g.64514520_64514534del NCBI36
NG_008305.1:g.53256_53270del , LRG_725:g.53256_53270del

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.116_130del ENSP00000508681.1:p.Gly39_Asp43del
ENST00000685172.1:c.182_196del ENSP00000509604.1:p.Gly61_Asp65del
ENST00000685763.1:c.182_196del ENSP00000509016.1:p.Gly61_Asp65del
ENST00000686347.1:c.182_196del ENSP00000509027.1:p.Gly61_Asp65del
ENST00000687191.1:n.618_632del
ENST00000689951.1:c.182_196del ENSP00000509308.1:p.Gly61_Asp65del
ENST00000691077.1:c.182_196del ENSP00000509843.1:p.Gly61_Asp65del
ENST00000691576.1:c.182_196del ENSP00000510066.1:p.Gly61_Asp65del
ENST00000691937.1:c.182_196del ENSP00000508768.1:p.Gly61_Asp65del
ENST00000692487.1:c.182_196del ENSP00000509534.1:p.Gly61_Asp65del
ENST00000692683.1:c.116_130del ENSP00000508437.1:p.Gly39_Asp43del
ENST00000693150.1:c.116_130del ENSP00000510309.1:p.Gly39_Asp43del
ENST00000307102.10:c.182_196del MANE Select ENSP00000302486.5:p.Gly61_Asp65del
ENST00000307102.9:c.182_196del ENSP00000302486.4:p.Gly61_Asp65del
ENST00000425818.2:n.693_707del
NM_002755.3:c.182_196del , LRG_725t1:c.182_196del NP_002746.1:p.Gly61_Asp65del
XM_011521783.1:c.116_130del XP_011520085.1:p.Gly39_Asp43del
XM_011521783.3:c.116_130del XP_011520085.1:p.Gly39_Asp43del
XM_017022411.2:c.182_196del XP_016877900.1:p.Gly61_Asp65del
XM_017022412.1:c.116_130del XP_016877901.1:p.Gly39_Asp43del
NM_002755.4:c.182_196del MANE Select NP_002746.1:p.Gly61_Asp65del
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