Canonical Allele Identifier: CA2184097347
Gene: MAP2K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66481695_66481739delinsCTTCTCTTCCCCAATCTACCTGTGTCAGTTCCCTCCTTTTCTATT , CM000677.2:g.66481695_66481739delinsCTTCTCTTCCCCAATCTACCTGTGTCAGTTCCCTCCTTTTCTATT GRCh38
NC_000015.9:g.66774033_66774077delinsCTTCTCTTCCCCAATCTACCTGTGTCAGTTCCCTCCTTTTCTATT , CM000677.1:g.66774033_66774077delinsCTTCTCTTCCCCAATCTACCTGTGTCAGTTCCCTCCTTTTCTATT GRCh37
NC_000015.8:g.64561087_64561131delinsCTTCTCTTCCCCAATCTACCTGTGTCAGTTCCCTCCTTTTCTATT NCBI36
NG_008305.1:g.99823_99867delinsCTTCTCTTCCCCAATCTACCTGTGTCAGTTCCCTCCTTTTCTATT , LRG_725:g.99823_99867delinsCTTCTCTTCCCCAATCTACCTGTGTCAGTTCCCTCCTTTTCTATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.503-60_503-16delinsCTTCTCTTCCCCAATCTACCTGTGTCAGTTCCCTCCTTTTCTATT ENSP00000508681.1:n.503-60_503-16delinsCTTCTCTTCCCCAATCTACCTG...
ENST00000685172.1:c.569-60_569-16delinsCTTCTCTTCCCCAATCTACCTGTGTCAGTTCCCTCCTTTTCTATT ENSP00000509604.1:n.569-60_569-16delinsCTTCTCTTCCCCAATCTACCTG...
ENST00000685763.1:c.422-60_422-16delinsCTTCTCTTCCCCAATCTACCTGTGTCAGTTCCCTCCTTTTCTATT ENSP00000509016.1:n.422-60_422-16delinsCTTCTCTTCCCCAATCTACCTG...
ENST00000686347.1:c.569-5533_569-5489delinsCTTCTCTTCCCCAATCTACCTGTGTCAGTTCCCTCCTTTTCTATT ENSP00000509027.1:n.569-5533_569-5489delinsCTTCTCTTCCCCAATCTA...
ENST00000687191.1:n.927-60_927-16delinsCTTCTCTTCCCCAATCTACCTGTGTCAGTTCCCTCCTTTTCTATT
ENST00000689951.1:c.620-60_620-16delinsCTTCTCTTCCCCAATCTACCTGTGTCAGTTCCCTCCTTTTCTATT ENSP00000509308.1:n.620-60_620-16delinsCTTCTCTTCCCCAATCTACCTG...
ENST00000691077.1:c.569-60_569-16delinsCTTCTCTTCCCCAATCTACCTGTGTCAGTTCCCTCCTTTTCTATT ENSP00000509843.1:n.569-60_569-16delinsCTTCTCTTCCCCAATCTACCTG...
ENST00000691576.1:c.569-3299_569-3255delinsCTTCTCTTCCCCAATCTACCTGTGTCAGTTCCCTCCTTTTCTATT ENSP00000510066.1:n.569-3299_569-3255delinsCTTCTCTTCCCCAATCTA...
ENST00000691937.1:c.569-60_569-16delinsCTTCTCTTCCCCAATCTACCTGTGTCAGTTCCCTCCTTTTCTATT ENSP00000508768.1:n.569-60_569-16delinsCTTCTCTTCCCCAATCTACCTG...
ENST00000692487.1:c.569-60_569-16delinsCTTCTCTTCCCCAATCTACCTGTGTCAGTTCCCTCCTTTTCTATT ENSP00000509534.1:n.569-60_569-16delinsCTTCTCTTCCCCAATCTACCTG...
ENST00000692683.1:c.503-60_503-16delinsCTTCTCTTCCCCAATCTACCTGTGTCAGTTCCCTCCTTTTCTATT ENSP00000508437.1:n.503-60_503-16delinsCTTCTCTTCCCCAATCTACCTG...
ENST00000693150.1:c.425-60_425-16delinsCTTCTCTTCCCCAATCTACCTGTGTCAGTTCCCTCCTTTTCTATT ENSP00000510309.1:n.425-60_425-16delinsCTTCTCTTCCCCAATCTACCTG...
ENST00000307102.10:c.569-60_569-16delinsCTTCTCTTCCCCAATCTACCTGTGTCAGTTCCCTCCTTTTCTATT MANE Select ENSP00000302486.5:n.569-60_569-16delinsCTTCTCTTCCCCAATCTACCTG...
ENST00000307102.9:c.569-60_569-16delinsCTTCTCTTCCCCAATCTACCTGTGTCAGTTCCCTCCTTTTCTATT ENSP00000302486.4:n.569-60_569-16delinsCTTCTCTTCCCCAATCTACCTG...
ENST00000566326.1:c.41-60_41-16delinsCTTCTCTTCCCCAATCTACCTGTGTCAGTTCCCTCCTTTTCTATT ENSP00000456438.1:n.41-60_41-16delinsCTTCTCTTCCCCAATCTACCTGTG...
NM_002755.3:c.569-60_569-16delinsCTTCTCTTCCCCAATCTACCTGTGTCAGTTCCCTCCTTTTCTATT , LRG_725t1:c.569-60_569-16delinsCTTCTCTTCCCCAATCTACCTGTGTCAGTTCCCTCCTTTTCTATT NP_002746.1:n.569-60_569-16delinsCTTCTCTTCCCCAATCTACCTGTGTCAG...
XM_011521783.1:c.503-60_503-16delinsCTTCTCTTCCCCAATCTACCTGTGTCAGTTCCCTCCTTTTCTATT XP_011520085.1:n.503-60_503-16delinsCTTCTCTTCCCCAATCTACCTGTGT...
XM_011521783.3:c.503-60_503-16delinsCTTCTCTTCCCCAATCTACCTGTGTCAGTTCCCTCCTTTTCTATT XP_011520085.1:n.503-60_503-16delinsCTTCTCTTCCCCAATCTACCTGTGT...
XM_017022411.2:c.491-60_491-16delinsCTTCTCTTCCCCAATCTACCTGTGTCAGTTCCCTCCTTTTCTATT XP_016877900.1:n.491-60_491-16delinsCTTCTCTTCCCCAATCTACCTGTGT...
XM_017022412.1:c.425-60_425-16delinsCTTCTCTTCCCCAATCTACCTGTGTCAGTTCCCTCCTTTTCTATT XP_016877901.1:n.425-60_425-16delinsCTTCTCTTCCCCAATCTACCTGTGT...
XM_017022413.1:c.41-60_41-16delinsCTTCTCTTCCCCAATCTACCTGTGTCAGTTCCCTCCTTTTCTATT XP_016877902.1:n.41-60_41-16delinsCTTCTCTTCCCCAATCTACCTGTGTCA...
NM_002755.4:c.569-60_569-16delinsCTTCTCTTCCCCAATCTACCTGTGTCAGTTCCCTCCTTTTCTATT MANE Select NP_002746.1:n.569-60_569-16delinsCTTCTCTTCCCCAATCTACCTGTGTCAG...