Canonical Allele Identifier: CA2184100226
Gene: MAP2K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66485265_66485291delinsGCTGATTCTCTGTACATTCTGCCAAGA , CM000677.2:g.66485265_66485291delinsGCTGATTCTCTGTACATTCTGCCAAGA GRCh38
NC_000015.9:g.66777603_66777629delinsGCTGATTCTCTGTACATTCTGCCAAGA , CM000677.1:g.66777603_66777629delinsGCTGATTCTCTGTACATTCTGCCAAGA GRCh37
NC_000015.8:g.64564657_64564683delinsGCTGATTCTCTGTACATTCTGCCAAGA NCBI36
NG_008305.1:g.103393_103419delinsGCTGATTCTCTGTACATTCTGCCAAGA , LRG_725:g.103393_103419delinsGCTGATTCTCTGTACATTCTGCCAAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.628-1963_628-1937delinsGCTGATTCTCTGTACATTCTGCCAAGA ENSP00000508681.1:n.628-1963_628-1937delinsGCTGATTCTCTGTACATT...
ENST00000685172.1:c.895+74_895+100delinsGCTGATTCTCTGTACATTCTGCCAAGA ENSP00000509604.1:n.895+74_895+100delinsGCTGATTCTCTGTACATTCTG...
ENST00000685763.1:c.748+74_748+100delinsGCTGATTCTCTGTACATTCTGCCAAGA ENSP00000509016.1:n.748+74_748+100delinsGCTGATTCTCTGTACATTCTG...
ENST00000686347.1:c.569-1963_569-1937delinsGCTGATTCTCTGTACATTCTGCCAAGA ENSP00000509027.1:n.569-1963_569-1937delinsGCTGATTCTCTGTACATT...
ENST00000687191.1:n.1253+74_1253+100delinsGCTGATTCTCTGTACATTCTGCCAAGA
ENST00000687481.1:n.310+74_310+100delinsGCTGATTCTCTGTACATTCTGCCAAGA
ENST00000689951.1:c.946+74_946+100delinsGCTGATTCTCTGTACATTCTGCCAAGA ENSP00000509308.1:n.946+74_946+100delinsGCTGATTCTCTGTACATTCTG...
ENST00000691077.1:c.*132+74_*132+100delinsGCTGATTCTCTGTACATTCTGCCAAGA ENSP00000509843.1:n.*132+74_*132+100delinsGCTGATTCTCTGTACATTC...
ENST00000691576.1:c.766+74_766+100delinsGCTGATTCTCTGTACATTCTGCCAAGA ENSP00000510066.1:n.766+74_766+100delinsGCTGATTCTCTGTACATTCTG...
ENST00000691937.1:c.895+74_895+100delinsGCTGATTCTCTGTACATTCTGCCAAGA ENSP00000508768.1:n.895+74_895+100delinsGCTGATTCTCTGTACATTCTG...
ENST00000692487.1:c.*132+74_*132+100delinsGCTGATTCTCTGTACATTCTGCCAAGA ENSP00000509534.1:n.*132+74_*132+100delinsGCTGATTCTCTGTACATTC...
ENST00000692683.1:c.829+74_829+100delinsGCTGATTCTCTGTACATTCTGCCAAGA ENSP00000508437.1:n.829+74_829+100delinsGCTGATTCTCTGTACATTCTG...
ENST00000693150.1:c.751+74_751+100delinsGCTGATTCTCTGTACATTCTGCCAAGA ENSP00000510309.1:n.751+74_751+100delinsGCTGATTCTCTGTACATTCTG...
ENST00000307102.10:c.895+74_895+100delinsGCTGATTCTCTGTACATTCTGCCAAGA MANE Select ENSP00000302486.5:n.895+74_895+100delinsGCTGATTCTCTGTACATTCTG...
ENST00000307102.9:c.895+74_895+100delinsGCTGATTCTCTGTACATTCTGCCAAGA ENSP00000302486.4:n.895+74_895+100delinsGCTGATTCTCTGTACATTCTG...
ENST00000566326.1:c.367+74_367+100delinsGCTGATTCTCTGTACATTCTGCCAAGA ENSP00000456438.1:n.367+74_367+100delinsGCTGATTCTCTGTACATTCTG...
NM_002755.3:c.895+74_895+100delinsGCTGATTCTCTGTACATTCTGCCAAGA , LRG_725t1:c.895+74_895+100delinsGCTGATTCTCTGTACATTCTGCCAAGA NP_002746.1:n.895+74_895+100delinsGCTGATTCTCTGTACATTCTGCCAAGA...
XM_011521783.1:c.829+74_829+100delinsGCTGATTCTCTGTACATTCTGCCAAGA XP_011520085.1:n.829+74_829+100delinsGCTGATTCTCTGTACATTCTGCCA...
XM_011521783.3:c.829+74_829+100delinsGCTGATTCTCTGTACATTCTGCCAAGA XP_011520085.1:n.829+74_829+100delinsGCTGATTCTCTGTACATTCTGCCA...
XM_017022411.2:c.817+74_817+100delinsGCTGATTCTCTGTACATTCTGCCAAGA XP_016877900.1:n.817+74_817+100delinsGCTGATTCTCTGTACATTCTGCCA...
XM_017022412.1:c.751+74_751+100delinsGCTGATTCTCTGTACATTCTGCCAAGA XP_016877901.1:n.751+74_751+100delinsGCTGATTCTCTGTACATTCTGCCA...
XM_017022413.1:c.367+74_367+100delinsGCTGATTCTCTGTACATTCTGCCAAGA XP_016877902.1:n.367+74_367+100delinsGCTGATTCTCTGTACATTCTGCCA...
NM_002755.4:c.895+74_895+100delinsGCTGATTCTCTGTACATTCTGCCAAGA MANE Select NP_002746.1:n.895+74_895+100delinsGCTGATTCTCTGTACATTCTGCCAAGA...