Canonical Allele Identifier: CA2804543903
Gene: MAP2K1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66435220_66435221insA , CM000677.2:g.66435220_66435221insA GRCh38
NC_000015.9:g.66727558_66727559insA , CM000677.1:g.66727558_66727559insA GRCh37
NC_000015.8:g.64514612_64514613insA NCBI36
NG_008305.1:g.53348_53349insA , LRG_725:g.53348_53349insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.208_209insA ENSP00000508681.1:p.Leu70HisfsTer29
ENST00000685172.1:c.274_275insA ENSP00000509604.1:p.Leu92HisfsTer29
ENST00000685763.1:c.274_275insA ENSP00000509016.1:p.Leu92HisfsTer23
ENST00000686347.1:c.274_275insA ENSP00000509027.1:p.Leu92HisfsTer29
ENST00000687191.1:n.710_711insA
ENST00000689951.1:c.274_275insA ENSP00000509308.1:p.Leu92HisfsTer29
ENST00000691077.1:c.274_275insA ENSP00000509843.1:p.Leu92HisfsTer29
ENST00000691576.1:c.274_275insA ENSP00000510066.1:p.Leu92HisfsTer29
ENST00000691937.1:c.274_275insA ENSP00000508768.1:p.Leu92HisfsTer29
ENST00000692487.1:c.274_275insA ENSP00000509534.1:p.Leu92HisfsTer29
ENST00000692683.1:c.208_209insA ENSP00000508437.1:p.Leu70HisfsTer29
ENST00000693150.1:c.208_209insA ENSP00000510309.1:p.Leu70HisfsTer29
ENST00000307102.10:c.274_275insA MANE Select ENSP00000302486.5:p.Leu92HisfsTer29
ENST00000307102.9:c.274_275insA ENSP00000302486.4:p.Leu92HisfsTer29
ENST00000425818.2:n.785_786insA
NM_002755.3:c.274_275insA , LRG_725t1:c.274_275insA NP_002746.1:p.Leu92HisfsTer29
XM_011521783.1:c.208_209insA XP_011520085.1:p.Leu70HisfsTer29
XM_011521783.3:c.208_209insA XP_011520085.1:p.Leu70HisfsTer29
XM_017022411.2:c.274_275insA XP_016877900.1:p.Leu92HisfsTer29
XM_017022412.1:c.208_209insA XP_016877901.1:p.Leu70HisfsTer29
NM_002755.4:c.274_275insA MANE Select NP_002746.1:p.Leu92HisfsTer29
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