Canonical Allele Identifier: CA2184071892
Gene: MAP2K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66435428_66435450delinsCGATTCTCCTGCCTCAGCCTCCT , CM000677.2:g.66435428_66435450delinsCGATTCTCCTGCCTCAGCCTCCT GRCh38
NC_000015.9:g.66727766_66727788delinsCGATTCTCCTGCCTCAGCCTCCT , CM000677.1:g.66727766_66727788delinsCGATTCTCCTGCCTCAGCCTCCT GRCh37
NC_000015.8:g.64514820_64514842delinsCGATTCTCCTGCCTCAGCCTCCT NCBI36
NG_008305.1:g.53556_53578delinsCGATTCTCCTGCCTCAGCCTCCT , LRG_725:g.53556_53578delinsCGATTCTCCTGCCTCAGCCTCCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.225+191_225+213delinsCGATTCTCCTGCCTCAGCCTCCT ENSP00000508681.1:n.225+191_225+213delinsCGATTCTCCTGCCTCAGCCT...
ENST00000685172.1:c.291+191_291+213delinsCGATTCTCCTGCCTCAGCCTCCT ENSP00000509604.1:n.291+191_291+213delinsCGATTCTCCTGCCTCAGCCT...
ENST00000685763.1:c.291+191_291+213delinsCGATTCTCCTGCCTCAGCCTCCT ENSP00000509016.1:n.291+191_291+213delinsCGATTCTCCTGCCTCAGCCT...
ENST00000686347.1:c.291+191_291+213delinsCGATTCTCCTGCCTCAGCCTCCT ENSP00000509027.1:n.291+191_291+213delinsCGATTCTCCTGCCTCAGCCT...
ENST00000687191.1:n.727+191_727+213delinsCGATTCTCCTGCCTCAGCCTCCT
ENST00000689951.1:c.291+191_291+213delinsCGATTCTCCTGCCTCAGCCTCCT ENSP00000509308.1:n.291+191_291+213delinsCGATTCTCCTGCCTCAGCCT...
ENST00000691077.1:c.291+191_291+213delinsCGATTCTCCTGCCTCAGCCTCCT ENSP00000509843.1:n.291+191_291+213delinsCGATTCTCCTGCCTCAGCCT...
ENST00000691576.1:c.291+191_291+213delinsCGATTCTCCTGCCTCAGCCTCCT ENSP00000510066.1:n.291+191_291+213delinsCGATTCTCCTGCCTCAGCCT...
ENST00000691937.1:c.291+191_291+213delinsCGATTCTCCTGCCTCAGCCTCCT ENSP00000508768.1:n.291+191_291+213delinsCGATTCTCCTGCCTCAGCCT...
ENST00000692487.1:c.291+191_291+213delinsCGATTCTCCTGCCTCAGCCTCCT ENSP00000509534.1:n.291+191_291+213delinsCGATTCTCCTGCCTCAGCCT...
ENST00000692683.1:c.225+191_225+213delinsCGATTCTCCTGCCTCAGCCTCCT ENSP00000508437.1:n.225+191_225+213delinsCGATTCTCCTGCCTCAGCCT...
ENST00000693150.1:c.225+191_225+213delinsCGATTCTCCTGCCTCAGCCTCCT ENSP00000510309.1:n.225+191_225+213delinsCGATTCTCCTGCCTCAGCCT...
ENST00000307102.10:c.291+191_291+213delinsCGATTCTCCTGCCTCAGCCTCCT MANE Select ENSP00000302486.5:n.291+191_291+213delinsCGATTCTCCTGCCTCAGCCT...
ENST00000307102.9:c.291+191_291+213delinsCGATTCTCCTGCCTCAGCCTCCT ENSP00000302486.4:n.291+191_291+213delinsCGATTCTCCTGCCTCAGCCT...
ENST00000425818.2:n.802+191_802+213delinsCGATTCTCCTGCCTCAGCCTCCT
NM_002755.3:c.291+191_291+213delinsCGATTCTCCTGCCTCAGCCTCCT , LRG_725t1:c.291+191_291+213delinsCGATTCTCCTGCCTCAGCCTCCT NP_002746.1:n.291+191_291+213delinsCGATTCTCCTGCCTCAGCCTCCT
XM_011521783.1:c.225+191_225+213delinsCGATTCTCCTGCCTCAGCCTCCT XP_011520085.1:n.225+191_225+213delinsCGATTCTCCTGCCTCAGCCTCCT...
XM_011521783.3:c.225+191_225+213delinsCGATTCTCCTGCCTCAGCCTCCT XP_011520085.1:n.225+191_225+213delinsCGATTCTCCTGCCTCAGCCTCCT...
XM_017022411.2:c.291+191_291+213delinsCGATTCTCCTGCCTCAGCCTCCT XP_016877900.1:n.291+191_291+213delinsCGATTCTCCTGCCTCAGCCTCCT...
XM_017022412.1:c.225+191_225+213delinsCGATTCTCCTGCCTCAGCCTCCT XP_016877901.1:n.225+191_225+213delinsCGATTCTCCTGCCTCAGCCTCCT...
NM_002755.4:c.291+191_291+213delinsCGATTCTCCTGCCTCAGCCTCCT MANE Select NP_002746.1:n.291+191_291+213delinsCGATTCTCCTGCCTCAGCCTCCT