Canonical Allele Identifier: CA2629081347
Gene: MAP2K1 HGNC NCBI

Linked Data

gnomAD v4: 15-66435276-T-TAAGTACCCTGAGAAATAATC
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66435276_66435277insAAGTACCCTGAGAAATAATC , CM000677.2:g.66435276_66435277insAAGTACCCTGAGAAATAATC GRCh38
NC_000015.9:g.66727614_66727615insAAGTACCCTGAGAAATAATC , CM000677.1:g.66727614_66727615insAAGTACCCTGAGAAATAATC GRCh37
NC_000015.8:g.64514668_64514669insAAGTACCCTGAGAAATAATC NCBI36
NG_008305.1:g.53404_53405insAAGTACCCTGAGAAATAATC , LRG_725:g.53404_53405insAAGTACCCTGAGAAATAATC

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.225+39_225+40insAAGTACCCTGAGAAATAATC ENSP00000508681.1:n.225+39_225+40insAAGTACCCTGAGAAATAATC
ENST00000685172.1:c.291+39_291+40insAAGTACCCTGAGAAATAATC ENSP00000509604.1:n.291+39_291+40insAAGTACCCTGAGAAATAATC
ENST00000685763.1:c.291+39_291+40insAAGTACCCTGAGAAATAATC ENSP00000509016.1:n.291+39_291+40insAAGTACCCTGAGAAATAATC
ENST00000686347.1:c.291+39_291+40insAAGTACCCTGAGAAATAATC ENSP00000509027.1:n.291+39_291+40insAAGTACCCTGAGAAATAATC
ENST00000687191.1:n.727+39_727+40insAAGTACCCTGAGAAATAATC
ENST00000689951.1:c.291+39_291+40insAAGTACCCTGAGAAATAATC ENSP00000509308.1:n.291+39_291+40insAAGTACCCTGAGAAATAATC
ENST00000691077.1:c.291+39_291+40insAAGTACCCTGAGAAATAATC ENSP00000509843.1:n.291+39_291+40insAAGTACCCTGAGAAATAATC
ENST00000691576.1:c.291+39_291+40insAAGTACCCTGAGAAATAATC ENSP00000510066.1:n.291+39_291+40insAAGTACCCTGAGAAATAATC
ENST00000691937.1:c.291+39_291+40insAAGTACCCTGAGAAATAATC ENSP00000508768.1:n.291+39_291+40insAAGTACCCTGAGAAATAATC
ENST00000692487.1:c.291+39_291+40insAAGTACCCTGAGAAATAATC ENSP00000509534.1:n.291+39_291+40insAAGTACCCTGAGAAATAATC
ENST00000692683.1:c.225+39_225+40insAAGTACCCTGAGAAATAATC ENSP00000508437.1:n.225+39_225+40insAAGTACCCTGAGAAATAATC
ENST00000693150.1:c.225+39_225+40insAAGTACCCTGAGAAATAATC ENSP00000510309.1:n.225+39_225+40insAAGTACCCTGAGAAATAATC
ENST00000307102.10:c.291+39_291+40insAAGTACCCTGAGAAATAATC MANE Select ENSP00000302486.5:n.291+39_291+40insAAGTACCCTGAGAAATAATC
ENST00000307102.9:c.291+39_291+40insAAGTACCCTGAGAAATAATC ENSP00000302486.4:n.291+39_291+40insAAGTACCCTGAGAAATAATC
ENST00000425818.2:n.802+39_802+40insAAGTACCCTGAGAAATAATC
NM_002755.3:c.291+39_291+40insAAGTACCCTGAGAAATAATC , LRG_725t1:c.291+39_291+40insAAGTACCCTGAGAAATAATC NP_002746.1:n.291+39_291+40insAAGTACCCTGAGAAATAATC
XM_011521783.1:c.225+39_225+40insAAGTACCCTGAGAAATAATC XP_011520085.1:n.225+39_225+40insAAGTACCCTGAGAAATAATC
XM_011521783.3:c.225+39_225+40insAAGTACCCTGAGAAATAATC XP_011520085.1:n.225+39_225+40insAAGTACCCTGAGAAATAATC
XM_017022411.2:c.291+39_291+40insAAGTACCCTGAGAAATAATC XP_016877900.1:n.291+39_291+40insAAGTACCCTGAGAAATAATC
XM_017022412.1:c.225+39_225+40insAAGTACCCTGAGAAATAATC XP_016877901.1:n.225+39_225+40insAAGTACCCTGAGAAATAATC
NM_002755.4:c.291+39_291+40insAAGTACCCTGAGAAATAATC MANE Select NP_002746.1:n.291+39_291+40insAAGTACCCTGAGAAATAATC
Search 100 bp 5'
Search 100 bp 3'